Kestra Medical Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-07-16
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P200037 | Wearable automated external defibrillator | MVK | 2026-07-16 | View |
| 510(k) | K233864 | ASSURE Wearable ECG | MWJ | 2024-05-07 | View |
No matching devices.