Amf Biological and Diagnostics Co.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K852418 | QCM-SP1(NORMAL CONCENTTRATION) & SP2(ABNORMAL) | JJY | 1985-07-15 | View |
| 510(k) | K821931 | ZETA-CORT | CGR | 1982-07-22 | View |
| 510(k) | K821553 | ZETAPHASE T3 UPTAKE DIAGNOSTIC KIT | KHQ | 1982-06-25 | View |
| 510(k) | K821554 | ZETAPHASE T4 RADIOIMMUNOASSAY DIAG. KIT | CDX | 1982-06-25 | View |
| 510(k) | K812329 | ZETA-SERA D | KIS | 1981-09-01 | View |
No matching devices.
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