Coagusense, Inc.
3 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-Testing (K212779) | Coagusense, Inc. | 2022-10-05 |
| Coag-Sense Prothrombin Time (PT) / INR Monitoring Device (K183255) | Coagusense, Inc. | 2019-02-21 |
| COAGUSENSE SELF-TEST PROTHROMBIN TIME/INR MONITORING SYSTEM (K093243) | Coagusense, Inc. | 2010-04-07 |
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