Accriva Diagnostics, Inc.
5 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2 recall (Z-2460-2026) | Accriva Diagnostics, Inc. | 2026-06-16 |
| Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the recall (Z-0880-2026) | Accriva Diagnostics, Inc. | 2025-12-03 |
| VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The Verif recall (Z-0500-2026) | Accriva Diagnostics, Inc. | 2025-11-13 |
| VerifyNow P2Y12 Platelet Reactivity Test, REF: 85064 recall (Z-0961-2025) | Accriva Diagnostics, Inc. | 2025-01-16 |
| AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated be recall (Z-0279-2025) | Accriva Diagnostics, Inc. | 2024-10-31 |
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Every clearance here is in the API, with alerts when new ones post.