Company ยท US
Amf Biological and Diagnostics Co.
FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1985. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 15, 1985 | K852418 | QCM-SP1(NORMAL CONCENTTRATION) & SP2(ABNORMAL) Amf Biological and Diagnostics Co. | JJY |
| Jul 22, 1982 | K821931 | ZETA-CORT Amf Biological and Diagnostics Co. | CGR |
| Jun 25, 1982 | K821554 | ZETAPHASE T4 RADIOIMMUNOASSAY DIAG. KIT Amf Biological and Diagnostics Co. | CDX |
| Jun 25, 1982 | K821553 | ZETAPHASE T3 UPTAKE DIAGNOSTIC KIT Amf Biological and Diagnostics Co. | KHQ |
| Sep 1, 1981 | K812329 | ZETA-SERA D Amf Biological and Diagnostics Co. | KIS |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||