E. R. Squibb & Sons, Inc.
FDA 510(k) & PMA Approved Devices — 32 products
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Total Devices32
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K821494 | RIA STAT 16 | JJJ | 1982-06-03 | View |
| 510(k) | K820616 | ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY | CIB | 1982-03-26 | View |
| 510(k) | K820341 | CORTISOL-SQUIBB RADIOIMMUNOASSAY KIT | CGR | 1982-03-04 | View |
| 510(k) | K820340 | T3 UPTAKE-SQUIBB DIAGNOSTIC KIT | KHQ | 1982-03-04 | View |
| 510(k) | K811240 | SUR-FIT LOOP OSTOMY O.R. SET | EXB | 1981-06-16 | View |
| 510(k) | K811239 | SUR-FIT DISPOSABLE CONVEX INSERT | EXB | 1981-06-09 | View |
| 510(k) | K811160 | SUR-FIT IRRIGATION SLEEVE | EXD | 1981-06-02 | View |
| 510(k) | K811163 | SUR-FIT DISPOSABLE FANGE CAP | EXB | 1981-05-21 | View |
| 510(k) | K810966 | DIAGOXIN SQUIBB RADIOIMMUNOASSAY KIT | DNL | 1981-04-21 | View |
| 510(k) | K810211 | T3 RIA KIT | CDP | 1981-02-10 | View |
| 510(k) | K803100 | STOMAHESIVE PASTE PROTECTIVE SKIN BARR | EZR | 1981-01-08 | View |
| 510(k) | K802883 | T3-SQUIBB RIA KIT | CDP | 1980-12-19 | View |
| 510(k) | K802456 | T4-SQUIBB RIA KIT | CDX | 1980-10-31 | View |
| 510(k) | K802455 | ESTRIOL-SQUIBB RIA KIT | CGI | 1980-10-31 | View |
| 510(k) | K802173 | URIHESIVE STRIPS | KNX | 1980-09-26 | View |
| 510(k) | K802172 | URIHESIVE SYSTEM | KNX | 1980-09-26 | View |
| 510(k) | K801703 | SUR-FIT SYSTEM STERILE O.R. SETS | EXB | 1980-09-09 | View |
| 510(k) | K801702 | SUR-FIT SYSTEM PRE-OPERATION SET | EXB | 1980-08-27 | View |
| 510(k) | K800997 | DIGOXIN CLASP RIA KIT | LCS | 1980-05-08 | View |
| 510(k) | K800495 | SUR-FIT UROSTOMY POUCH & URINARY BAG | EXB | 1980-04-08 | View |
No matching devices.
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