Retmap, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2026-04-01
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253586 | RM Electrode (RMH 25-01) | HLZ | 2026-04-01 | View |
| 510(k) | K232273 | RM Electrode (RMH 23-01) | HLZ | 2023-12-07 | View |
No matching devices.