Epimed International, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2020-04-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K200624 | Percutaneous Introducer | BSO | 2020-04-27 | View |
| 510(k) | K190256 | Rulo Radiofrequency Lesion Probe | GXI | 2019-03-08 | View |
No matching devices.