Suite 201, National Innovation Centre
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2026-07-30
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261410 | Navbit MARQ (PRD-001-SUP (Supine Registration Kit), PRD-001-LAT (Lateral Registration Kit)) | OLO | 2026-07-30 | View |
No matching devices.