Omni-Guide Holdings, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2023-04-21
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K230819 | OmniGuide RFID Surgical Laser Fibers | GEX | 2023-04-21 | View |
| 510(k) | K220189 | LISA Laser Surgical Fibers | GEX | 2022-04-29 | View |
No matching devices.