Richard-Allan Medical Ind., Inc.
Mchenry, IL, US
Richard-Allan Medical Ind., Inc. appears in FDA device records in Mchenry, IL. FDA records list 33 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 33
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 33 510(k) clearances for Richard-Allan Medical Ind., Inc. between 1977 and 1994. The busiest year on record is 1981, with 12. The most recent is 1994, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 3 |
| 1979 | 2 |
| 1981 | 12 |
| 1982 | 1 |
| 1983 | 4 |
| 1986 | 3 |
| 1987 | 1 |
| 1989 | 1 |
| 1990 | 2 |
| 1993 | 2 |
| 1994 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K931879 | REFLEX HTR | GCJ | Substantially Equivalent | |
| K924200 | REFLEX(R) ESC | KNF | Substantially Equivalent | |
| K926297 | REFLEX ESI | GEI | Substantially Equivalent | |
| K924761 | STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELD | GCJ | Substantially Equivalent | |
| K900566 | RICHARD-ALLAN VESSEL LOOPS | KDC | Substantially Equivalent | |
| K896262 | TITANIUM LIGATING CLIPS | HBT | Substantially Equivalent | |
| K890314 | PROTECTOR (SURGICAL INSTRUMENT) | MMK | Substantially Equivalent | |
| K873309 | REFLEX(TM) CA-T CLIP APPLIER | FZP | Substantially Equivalent | |
| K862404 | REFLEX(TM) CLIP APPLIER | FZP | Substantially Equivalent | |
| K862223 | MICRO THIN* PARAFFIN | KEO | Substantially Equivalent | |
| K861890 | 100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2 | PPM | Substantially Equivalent | |
| K832451 | CLEAR-RITE 3 | KEM | Substantially Equivalent | |
| K830867 | REFLEX ONE STAPLE EXTRACTOR | Substantially Equivalent | ||
| K830627 | CLARIFIER-RICHARD-ALLAN | KEM | Substantially Equivalent | |
| K830625 | CYTO-STAIN | HJQ | Substantially Equivalent | |
| K822145 | COMPLETE | FZQ | Substantially Equivalent | |
| K812847 | XYLENE | KEM | Substantially Equivalent | |
| K812846 | CLEAR-RITE II | KEM | Substantially Equivalent | |
| K811800 | BLUING REAGENT | PPM | Substantially Equivalent | |
| K811799 | CLEAR-MOUNT | LEB | Substantially Equivalent | |
| K811793 | FIX-RIGHT 90ML & 180 ML PREFILLED CONT | KDT | Substantially Equivalent | |
| K811802 | HEMATOXYLIN | HYJ | Substantially Equivalent | |
| K811801 | CAL-RITE | KDX | Substantially Equivalent | |
| K811798 | CLEAR-RITE | KEM | Substantially Equivalent | |
| K811797 | EOSIN-Y | HYB | Substantially Equivalent | |
| K811796 | FORMAL ALCOHOL | PPM | Substantially Equivalent | |
| K811795 | 10% NEUTRAL BUFFERED FORMALDEHYDE | IFP | Substantially Equivalent | |
| K811794 | 37% FORMALDEHYDE | IGG | Substantially Equivalent | |
| K790661 | PROTECTOR II | MMK | Substantially Equivalent | |
| K790660 | SURGICAL RULER | FTY | Substantially Equivalent | |
| K771611 | PROTECTOR | MMK | Substantially Equivalent | |
| K761323 | SURGICAL MARKING PEN | FZZ | Substantially Equivalent | |
| K761322 | SURGICAL BLADES | GES | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KEMAgent, Clearing
- HBTApplier, Hemostatic Clip
- GESBlade, Scalpel
- FZPClip, Implantable
- FZQClip, Removable (Skin)
- KNFCoagulator-Cutter, Endoscopic, Unipolar (And Accessories)
- MMKContainer, Sharps
- KDTContainer, Specimen Mailer And Storage, Sterile
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- HYBEosin Y
- IGGFormaldehyde (Formalin, Formol)
- IFPFormalin, Neutral Buffered
- KEOFormulations, Paraffin, All
- PPMGeneral Purpose Reagent
- HYJHematoxylin
- KDCInstrument, Surgical, Disposable
- GCJLaparoscope, General & Plastic Surgery
- FZZMarker, Skin
- LEBMounting Media
- KDXSolution, Decalcifier, Acid Containing
- HJQStereoscope, Ac-Powered
- FTYTape, Measuring, Rulers And Calipers
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