Helena Laboratories, Corp.
2 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Serrated Blade Applicator Kit (12 Sample), REF: 552687, For use with the Spife Nexus syste recall (Z-1975-2023) | Helena Laboratories, Corp. | 2023-06-16 |
| Cascade Abrazo aPTT Test Card, Model 5722, For Export Only. The firm name on the label is recall (Z-2761-2019) | Helena Laboratories, Corp. | 2019-09-27 |
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Every clearance here is in the API, with alerts when new ones post.