CERENOVUS, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2026-08-13
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K262398 | CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set | NRY | 2026-08-13 | View |
No matching devices.