NERL Diagnostics Corporation
2 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Lifesign Staph Latex Kits, 6 ml For In Vitro Diagnostic Use Catalog Number: 50051 Manufact recall (Z-1110-2010) | NERL Diagnostics Corporation | 2010-03-12 |
| Wampole Staph Latex Test, 6.0 ml -120 Test Kit For In Vitro Diagnostic Use Catalog Number: recall (Z-1111-2010) | NERL Diagnostics Corporation | 2010-03-12 |
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Every clearance here is in the API, with alerts when new ones post.