Biokit U.S.A. Inc.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Biokit HSV-2 Rapid test Catalogue Number: 3000-28001. 20 test Kit. In Vitro Diagnostic tes recall (Z-1970-2010) | Biokit U.S.A. Inc. | 2010-07-08 |
| Sure-Vue HSV-2 Rapid Test, Catalogue No: 23-046395. 20 test Kit In Vitro Diagnostic test f recall (Z-1971-2010) | Biokit U.S.A. Inc. | 2010-07-08 |
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Every clearance here is in the API, with alerts when new ones post.