Coagusense, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2022-10-05
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K212779 | Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-Testing | GJS | 2022-10-05 | View |
| 510(k) | K183255 | Coag-Sense Prothrombin Time (PT) / INR Monitoring Device | GJS | 2019-02-21 | View |
No matching devices.