Burroughs Wellcome Co.
FDA 510(k) & PMA Approved Devices — 17 products
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Total Devices17
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K820069 | WELLCOGEN GROUP B | GTZ | 1982-02-18 | View |
| 510(k) | K813508 | SAC-CEL | KTS | 1981-12-29 | View |
| 510(k) | K810215 | DAC-CEL HCG | JHI | 1981-04-17 | View |
| 510(k) | K810214 | DAC-CEL DIAGNATAL | JHI | 1981-03-06 | View |
| 510(k) | K810212 | DAC-CEL T3 UPTAKE | KHQ | 1981-02-10 | View |
| 510(k) | K810213 | DAC-CEL TSH | JLW | 1981-02-10 | View |
| 510(k) | K791231 | DAC-CEL T4 | CDX | 1979-09-04 | View |
| 510(k) | K791232 | DAC-CEL T3 | CDP | 1979-09-04 | View |
| 510(k) | K781607 | STREP-TEX | GTZ | 1978-10-17 | View |
| 510(k) | K780874 | THYMUNE-T | DDC | 1978-06-14 | View |
| 510(k) | K780873 | THYMUNE-M | DDC | 1978-06-14 | View |
| 510(k) | K780475 | DAC-CEL DIGOXIN RADIOIMMUNOASSAY KIT | DON | 1978-04-24 | View |
| 510(k) | K771560 | TOXHA TEST | GMM | 1977-09-15 | View |
| 510(k) | K771583 | FLUORESCENT ANTI. ANTI-HUMAN C3 | DAC | 1977-09-02 | View |
| 510(k) | K771562 | AGGLUTINATING SERUM W135 | GTJ | 1977-08-25 | View |
| 510(k) | K771139 | CRP-WELLCOTEST | DCN | 1977-07-14 | View |
| 510(k) | K770269 | CAMMADISK DIGOXIN | DON | 1977-03-16 | View |
No matching devices.
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