E. R. Squibb & Sons, Inc.
New York, NY, US
E. R. Squibb & Sons, Inc. appears in FDA device records in New York, NY. FDA records list 32 510(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
- 32
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 32 510(k) clearances for E. R. Squibb & Sons, Inc. between 1977 and 1982. The busiest year on record is 1980, with 9. The most recent is 1982, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 3 |
| 1978 | 5 |
| 1979 | 4 |
| 1980 | 9 |
| 1981 | 7 |
| 1982 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K821494 | RIA STAT 16 | JJJ | Substantially Equivalent | |
| K820616 | ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY | CIB | Substantially Equivalent | |
| K820341 | CORTISOL-SQUIBB RADIOIMMUNOASSAY KIT | CGR | Substantially Equivalent | |
| K820340 | T3 UPTAKE-SQUIBB DIAGNOSTIC KIT | KHQ | Substantially Equivalent | |
| K811240 | SUR-FIT LOOP OSTOMY O.R. SET | EXB | Substantially Equivalent | |
| K811239 | SUR-FIT DISPOSABLE CONVEX INSERT | EXB | Substantially Equivalent | |
| K811160 | SUR-FIT IRRIGATION SLEEVE | EXD | Substantially Equivalent | |
| K811163 | SUR-FIT DISPOSABLE FANGE CAP | EXB | Substantially Equivalent | |
| K810966 | DIAGOXIN SQUIBB RADIOIMMUNOASSAY KIT | DNL | Substantially Equivalent | |
| K810211 | T3 RIA KIT | CDP | Substantially Equivalent | |
| K803100 | STOMAHESIVE PASTE PROTECTIVE SKIN BARR | EZR | Substantially Equivalent | |
| K802883 | T3-SQUIBB RIA KIT | CDP | Substantially Equivalent | |
| K802456 | T4-SQUIBB RIA KIT | CDX | Substantially Equivalent | |
| K802455 | ESTRIOL-SQUIBB RIA KIT | CGI | Substantially Equivalent | |
| K802173 | URIHESIVE STRIPS | KNX | Substantially Equivalent | |
| K802172 | URIHESIVE SYSTEM | KNX | Substantially Equivalent | |
| K801703 | SUR-FIT SYSTEM STERILE O.R. SETS | EXB | Substantially Equivalent | |
| K801702 | SUR-FIT SYSTEM PRE-OPERATION SET | EXB | Substantially Equivalent | |
| K800997 | DIGOXIN CLASP RIA KIT | LCS | Substantially Equivalent | |
| K800495 | SUR-FIT UROSTOMY POUCH & URINARY BAG | EXB | Substantially Equivalent | |
| K792382 | STOMAHESIVE POWDER | EXB | Substantially Equivalent | |
| K790477 | TY RIA KIT, AUTOMATED ASSAY SYSTEM | CDX | Substantially Equivalent | |
| K790417 | T3 UPTAKE KIT | KHQ | Substantially Equivalent | |
| K790268 | CORTISOL RIA KIT | CGR | Substantially Equivalent | |
| K781660 | RIA, DIGOXIN | DON | Substantially Equivalent | |
| K781659 | ASSAY SYSTEM, GAMMAFLO, AUTOMATED | Substantially Equivalent | ||
| K781088 | OSTOMY APPLIANCE BELT | EXB | Substantially Equivalent | |
| K780511 | SNAP-FIT | EXB | Substantially Equivalent | |
| K780454 | ACTIVE-LIFE | EXB | Substantially Equivalent | |
| K771142 | T3 CLASP RIA KIT | CDP | Substantially Equivalent | |
| K770915 | CLASP RIA KIT, HTSH | JLW | Substantially Equivalent | |
| K770069 | DIGOXIN CLASP TM RIA KIT | DPO | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- EZRCement, Stomal Appliance, Ostomy
- EXBCollector, Ostomy
- KNXCollector, Urine, (And Accessories) For Indwelling Catheter
- JJJCounter (Beta, Gamma) For Clinical Use
- EXDIrrigator, Ostomy
- KHQRadioassay, Triiodothyronine Uptake
- CIBRadioimmunoassay, Angiotensin I And Renin
- CGRRadioimmunoassay, Cortisol
- LCSRadioimmunoassay, Digoxin (125-I)
- DPORadioimmunoassay, Digoxin (125-I), Rabbit Antibody, Coated Tube Sep.
- DNLRadioimmunoassay, Digoxin (125-I), Rabbit Antibody, Second Antibody Sep.
- DONRadioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.
- CGIRadioimmunoassay, Estriol
- JLWRadioimmunoassay, Thyroid-Stimulating Hormone
- CDXRadioimmunoassay, Total Thyroxine
- CDPRadioimmunoassay, Total Triiodothyronine
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain