Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K983886 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| biokitHSV-2 Rapid Test, REF: 300028001 | 2 | 01/26/2023 | Biokit, S.A. |
| Biokit HSV-2 Rapid test Catalogue Number: 3000-28001. 20 test Kit. In Vitro Diagnostic test fo... | 2 | 07/08/2010 | Biokit U.S.A. Inc. |
| Sure-Vue HSV-2 Rapid Test, Catalogue No: 23-046395. 20 test Kit In Vitro Diagnostic test for Herp... | 2 | 07/08/2010 | Biokit U.S.A. Inc. |
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