G.D. Searle and Co.
FDA 510(k) & PMA Approved Devices — 56 products
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Total Devices56
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K821159 | IN-LINE OXYGEN MONITORING SYSTEM | DRY | 1982-05-25 | View |
| 510(k) | K811068 | BYPASS COIL | KPY | 1981-05-27 | View |
| 510(k) | K811071 | VENOUS OXYGEN PROBE | CCE | 1981-05-05 | View |
| 510(k) | K803238 | INTRAVASCULAR CATHETER | FOZ | 1981-04-23 | View |
| 510(k) | K810630 | SILICONE ELASTOMER COATED LATEX FOLEY | KOD | 1981-03-31 | View |
| 510(k) | K810131 | ADMINISTRATION SET | FPD | 1981-02-26 | View |
| 510(k) | K802485 | SEARLE VASCULAR LOOPS | KDC | 1981-02-12 | View |
| 510(k) | K801805 | METRONIDAZOLE DISCS | JWY | 1981-02-10 | View |
| 510(k) | K810112 | SWR DISPOSABLE PREP RAZOR | KDC | 1981-02-04 | View |
| 510(k) | K802280 | WHITE KNIGHT DRAPE SEAL | KKX | 1980-10-10 | View |
| 510(k) | K802213 | WHITE KNIGHT BOVIE CORD/SUCTION TUBE | KKX | 1980-10-10 | View |
| 510(k) | K801415 | LATEX FOLEY CATHETER (HYDROMER COATED) | KOD | 1980-08-20 | View |
| 510(k) | K801414 | ERYTHROCATH INTRAVENOUS CATHETER PLA. U. | FOZ | 1980-08-13 | View |
| 510(k) | K800815 | ENTERAL & NASOGASTRIC SOL. ADMIN. SET | KNT | 1980-07-21 | View |
| 510(k) | K800928 | WHITE KNIGHT SUPPLEMENTAL DRAPE | KKX | 1980-05-20 | View |
| 510(k) | K800929 | WHITE KNIGHT SURGICAL PACK | FYA | 1980-05-20 | View |
| 510(k) | K800927 | WHITE KNIGHT DISP. STERILE BACK GOWN | FYA | 1980-05-20 | View |
| 510(k) | K800609 | CATHETER STYLET | KOD | 1980-04-10 | View |
| 510(k) | K800610 | URETHRAL SOUND | KOE | 1980-04-08 | View |
| 510(k) | K800611 | BOUGIE A BOULE | KOE | 1980-04-08 | View |
No matching devices.
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