Us Medical Innovations, LLC
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest FDA decision2024-05-03
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240297 | Canady Helios Cold Plasma™ XL-1000CP™ Ablation System (XL-1000CPSYS) | OAB | 2024-05-03 | View |
| 510(k) | K212736 | Canady Flex RoboWrist | GCJ | 2022-11-22 | View |
| 510(k) | K192124 | Canady Plasma SMART XL-1000 Electrosurgical Generator with Accessories | GEI | 2019-11-21 | View |
No matching devices.