Company ยท US
E. R. Squibb & Sons, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1982. Name variants (Inc, Corp, punctuation) are merged.
32510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| EXB | Collector, Ostomy | 10 |
| CDP | Radioimmunoassay, Total Triiodothyronine | 3 |
| CDX | Radioimmunoassay, Total Thyroxine | 2 |
| CGR | Radioimmunoassay, Cortisol | 2 |
| KHQ | Radioassay, Triiodothyronine Uptake | 2 |
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | 2 |
| CGI | Radioimmunoassay, Estriol | 1 |
| CIB | Radioimmunoassay, Angiotensin I And Renin | 1 |
| DNL | Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Second Antibody Sep. | 1 |
| DON | Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep. | 1 |
| DPO | Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Coated Tube Sep. | 1 |
| EXD | Irrigator, Ostomy | 1 |
| EZR | Cement, Stomal Appliance, Ostomy | 1 |
| JJJ | Counter (Beta, Gamma) For Clinical Use | 1 |
| JLW | Radioimmunoassay, Thyroid-Stimulating Hormone | 1 |
| LCS | Radioimmunoassay, Digoxin (125-I) | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 3, 1982 | K821494 | RIA STAT 16 E. R. Squibb & Sons, Inc. | JJJ |
| Mar 26, 1982 | K820616 | ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY E. R. Squibb & Sons, Inc. | CIB |
| Mar 4, 1982 | K820341 | CORTISOL-SQUIBB RADIOIMMUNOASSAY KIT E. R. Squibb & Sons, Inc. | CGR |
| Mar 4, 1982 | K820340 | T3 UPTAKE-SQUIBB DIAGNOSTIC KIT E. R. Squibb & Sons, Inc. | KHQ |
| Jun 16, 1981 | K811240 | SUR-FIT LOOP OSTOMY O.R. SET E. R. Squibb & Sons, Inc. | EXB |
| Jun 9, 1981 | K811239 | SUR-FIT DISPOSABLE CONVEX INSERT E. R. Squibb & Sons, Inc. | EXB |
| Jun 2, 1981 | K811160 | SUR-FIT IRRIGATION SLEEVE E. R. Squibb & Sons, Inc. | EXD |
| May 21, 1981 | K811163 | SUR-FIT DISPOSABLE FANGE CAP E. R. Squibb & Sons, Inc. | EXB |
| Apr 21, 1981 | K810966 | DIAGOXIN SQUIBB RADIOIMMUNOASSAY KIT E. R. Squibb & Sons, Inc. | DNL |
| Feb 10, 1981 | K810211 | T3 RIA KIT E. R. Squibb & Sons, Inc. | CDP |
| Jan 8, 1981 | K803100 | STOMAHESIVE PASTE PROTECTIVE SKIN BARR E. R. Squibb & Sons, Inc. | EZR |
| Dec 19, 1980 | K802883 | T3-SQUIBB RIA KIT E. R. Squibb & Sons, Inc. | CDP |
| Oct 31, 1980 | K802456 | T4-SQUIBB RIA KIT E. R. Squibb & Sons, Inc. | CDX |
| Oct 31, 1980 | K802455 | ESTRIOL-SQUIBB RIA KIT E. R. Squibb & Sons, Inc. | CGI |
| Sep 26, 1980 | K802173 | URIHESIVE STRIPS E. R. Squibb & Sons, Inc. | KNX |
| Sep 26, 1980 | K802172 | URIHESIVE SYSTEM E. R. Squibb & Sons, Inc. | KNX |
| Sep 9, 1980 | K801703 | SUR-FIT SYSTEM STERILE O.R. SETS E. R. Squibb & Sons, Inc. | EXB |
| Aug 27, 1980 | K801702 | SUR-FIT SYSTEM PRE-OPERATION SET E. R. Squibb & Sons, Inc. | EXB |
| May 8, 1980 | K800997 | DIGOXIN CLASP RIA KIT E. R. Squibb & Sons, Inc. | LCS |
| Apr 8, 1980 | K800495 | SUR-FIT UROSTOMY POUCH & URINARY BAG E. R. Squibb & Sons, Inc. | EXB |
| Dec 20, 1979 | K792382 | STOMAHESIVE POWDER E. R. Squibb & Sons, Inc. | EXB |
| Apr 26, 1979 | K790477 | TY RIA KIT, AUTOMATED ASSAY SYSTEM E. R. Squibb & Sons, Inc. | CDX |
| Apr 20, 1979 | K790417 | T3 UPTAKE KIT E. R. Squibb & Sons, Inc. | KHQ |
| Apr 4, 1979 | K790268 | CORTISOL RIA KIT E. R. Squibb & Sons, Inc. | CGR |
| Oct 24, 1978 | K781660 | RIA, DIGOXIN E. R. Squibb & Sons, Inc. | DON |
| Oct 24, 1978 | K781659 | ASSAY SYSTEM, GAMMAFLO, AUTOMATED E. R. Squibb & Sons, Inc. | |
| Aug 18, 1978 | K781088 | OSTOMY APPLIANCE BELT E. R. Squibb & Sons, Inc. | EXB |
| Apr 21, 1978 | K780511 | SNAP-FIT E. R. Squibb & Sons, Inc. | EXB |
| Apr 21, 1978 | K780454 | ACTIVE-LIFE E. R. Squibb & Sons, Inc. | EXB |
| Jul 14, 1977 | K771142 | T3 CLASP RIA KIT E. R. Squibb & Sons, Inc. | CDP |
| Jun 14, 1977 | K770915 | CLASP RIA KIT, HTSH E. R. Squibb & Sons, Inc. | JLW |
| Jan 18, 1977 | K770069 | DIGOXIN CLASP TM RIA KIT E. R. Squibb & Sons, Inc. | DPO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||