Pharmacia, Inc.
Mchenry, IL, US
Pharmacia, Inc. appears in FDA device records in Mchenry, IL. FDA records list 129 510(k) clearances between and , one PMA record and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 129
- PMA records
- 1
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
Showing 50 of 129FDA records hold 129 510(k) clearances for Pharmacia, Inc. between 1976 and 1998. The busiest year on record is 1988, with 17. The most recent is 1998, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1977 | 3 |
| 1980 | 4 |
| 1981 | 6 |
| 1982 | 4 |
| 1983 | 15 |
| 1984 | 14 |
| 1985 | 16 |
| 1986 | 7 |
| 1987 | 12 |
| 1988 | 17 |
| 1989 | 9 |
| 1990 | 7 |
| 1991 | 4 |
| 1995 | 3 |
| 1996 | 2 |
| 1997 | 4 |
| 1998 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K974350 | ALLERGAN IMMUNO CAP M4, M8, K70 | DHB | Substantially Equivalent | |
| K972364 | UNICAP PHADIATOP | DHB | Substantially Equivalent | |
| K972068 | UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82 | DHB | Substantially Equivalent | |
| K970420 | MASTERCAP AM 5.0/MASTERCAP RM 5.0 | JQW | Substantially Equivalent | |
| K964152 | UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMH | DGC | Substantially Equivalent | |
| K962274 | UNICAP 100 | DHB | Substantially Equivalent | |
| K941993 | PHARMACIA CAP SYSTEM PHADIATOP FEIA | DHB | Substantially Equivalent | |
| K954337 | GENOTROPIN MIXER | FMF | Substantially Equivalent | |
| K951025 | PISTON SYRINGE | FMF | Substantially Equivalent | |
| K952025 | ROBOCAP | JQW | Substantially Equivalent | |
| K911903 | ALLERGANS PHARMACIA CAP SYS.RAST RIA/FEIA | DHB | Substantially Equivalent | |
| K911631 | PHARMACIA SPECIFIC IGE CONTROL | DGC | Substantially Equivalent | |
| K910517 | CAP SYSTEM RAST ASM/RIA AND ASM/FEIA | DHB | Substantially Equivalent | |
| K905710 | PHARMACIA DELFIA NEONATAL HTSH KIT | JLW | Substantially Equivalent | |
| K902171 | MINISPACE(TM) IUI CATHETER | HDR | Substantially Equivalent | |
| K903578 | PHARMACIA DELFIA SYSTEM B2-MICRO | JZG | Substantially Equivalent | |
| K902358 | MODIFIED DELFIA ESTRADIOL KIT | CHP | Substantially Equivalent | |
| K900308 | SPERM SELECT SYSTEM | HDR | Substantially Equivalent | |
| K900240 | DELFIA TBG KIT | CEE | Substantially Equivalent | |
| K900449 | PHARMACIA B2 MICRO EIA | JZG | Substantially Equivalent | |
| K894190 | PHARMACIA CAP SYSTEM RAST RIA & RAST FEIA | DHB | Substantially Equivalent | |
| K895240 | DELFIA PLATE FLUOROMETER 1232 | KHO | Substantially Equivalent | |
| K894605 | DELFIA FREE THYROXINE (FT4) KIT | CEC | Substantially Equivalent | |
| K893951 | PHARMACIA CAP SYSTEM IGE RIA AND FEIA | DGC | Substantially Equivalent | |
| K893132 | PHADEBAS RAST(R)/PHADEZYM(R) RAST ALLERGEN DISC | DHB | Substantially Equivalent | |
| K891135 | PHADIATOP PAEDIATRIC RIA AND EIA | DHB | Substantially Equivalent | |
| K884809 | DELFIA SHBG KIT | CDZ | Substantially Equivalent | |
| K883814 | DELFIA HLH SPEC KIT | CEP | Substantially Equivalent | |
| K890428 | DELFIA PROGESTERONE KIT | JLS | Substantially Equivalent | |
| K880752 | PHADEBACT SHIGELLA TEST | GNB | Substantially Equivalent | |
| K883559 | DELFIA THYROXINE (T4) KIT | CDX | Substantially Equivalent | |
| K883810 | DELFIA TRIIODOTHYRONINE (T3) KIT | CDP | Substantially Equivalent | |
| K884545 | DELFIA (TM) HIGE KIT | DGC | Substantially Equivalent | |
| K883435 | NOVASPEC II SPECTROPHOTOMETER | JJQ | Substantially Equivalent | |
| K881627 | DELFIA(TM) NEONATAL HTSH KIT | JLW | Substantially Equivalent | |
| K874288 | PHADEBACT ETEC-LT TEST | GNA | Substantially Equivalent | |
| K882676 | PHARMACIA CHLAMYDIA EIA | LJC | Substantially Equivalent | |
| K882625 | PHARMACIA IGE RIA ULTRA | DGC | Substantially Equivalent | |
| K882626 | PHARMACIA IGE EIA ULTRA | DGC | Substantially Equivalent | |
| K882616 | ALTERNATE PROCEDURE, PHARMACIA IGE EIA | JHR | Substantially Equivalent | |
| K882173 | DELFIA ESTRADIOL KIT | CHP | Substantially Equivalent | |
| K881892 | PHARMACIA IGE RIACT | DGC | Substantially Equivalent | |
| K880899 | PHARMACIA IGG RAST RIA/PHARMACIA IGG RAST EIA | DHB | Substantially Equivalent | |
| K880719 | PHARMACIA B2-MICRO RIA | JZG | Substantially Equivalent | |
| K872573 | PHARMACLUSIVE (TM) | NAD | Substantially Equivalent | |
| K872572 | PHARMANET (TM) | EFQ | Substantially Equivalent for Some Indications | |
| K872453 | DEBRISAN ABSORBENT PAD | KOZ | Substantially Equivalent for Some Indications | |
| K873112 | PHADEBAS RAST/PHADEZYM RAST ALLERGEN DISC | DHB | Substantially Equivalent | |
| K873077 | PHARMACIA IGE EIA | JHR | Substantially Equivalent | |
| K872946 | PHADEBAS RAST/PHADEZYM RAST ALLERGEN DISC | DHB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GTYAntigens, All Groups, Streptococcus Spp.
- GTJAntisera, All Groups, N. Meningitidis
- GTZAntisera, All Groups, Streptococcus Spp.
- GNAAntisera, All Types, Escherichia Coli
- GNBAntisera, All Types, Shigella Spp.
- GWCAntisera, All Types, Streptococcus Pneumoniae
- GROAntisera, Fluorescent, All Types, Hemophilus Spp.
- LICAntiserum, Coagglutination (Direct) Neisseria Gonorrhoeae
- KOZBeads, Hydrophilic, For Wound Exudate Absorption
- HMXCannula, Ophthalmic
- HDRCap, Cervical
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- JJQColorimeter, Photometer, Spectrophotometer For Clinical Use
- NADDressing, Wound, Occlusive
- LJCEnzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)
- KHOFluorometer, For Clinical Use
- EFQGauze/Sponge, Internal
- DGCIge, Antigen, Antiserum, Control
- DEWIgg, Antigen, Antiserum, Control
- HQLIntraocular Lens
- JSXKit, Identification, Neisseria Gonorrhoeae
- MQLMedia, Reproductive
- BSPNeedle, Conduction, Anesthetic (W/Wo Introducer)
- JGZO-Phthalaldehyde, Urea Nitrogen
- LLDPort & Catheter, Implanted, Subcutaneous, Intraperitoneal
- LJTPort & Catheter, Implanted, Subcutaneous, Intravascular
- FRNPump, Infusion
- KHQRadioassay, Triiodothyronine Uptake
- LCSRadioimmunoassay, Digoxin (125-I)
- CHPRadioimmunoassay, Estradiol
- CECRadioimmunoassay, Free Thyroxine
- JHRRadioimmunoassay, Immunoglobulins (D, E)
- CFPRadioimmunoassay, Immunoreactive Insulin
- CEPRadioimmunoassay, Luteinizing Hormone
- JLSRadioimmunoassay, Progesterone
- CDZRadioimmunoassay, Testosterones And Dihydrotestosterone
- JLWRadioimmunoassay, Thyroid-Stimulating Hormone
- CEERadioimmunoassay, Thyroxine-Binding Globulin
- CDXRadioimmunoassay, Total Thyroxine
- CDPRadioimmunoassay, Total Triiodothyronine
- FPASet, Administration, Intravascular
- JJXSingle (Specified) Analyte Controls (Assayed And Unassayed)
- CIWStarch-Dye Bound Polymer, Amylase
- JQWStation, Pipetting And Diluting, For Clinical Use
- FMFSyringe, Piston
- JZGSystem, Test, Beta-2-Microglobulin Immunological
- DHBSystem, Test, Radioallergosorbent (Rast) Immunological
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain
