JMS North America Corporation
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2025-08-15
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251877 | JMS CAVEO A.V. Fistula Needle Set | FIE | 2025-08-15 | View |
| 510(k) | K172499 | NEOSHIELD | ONB | 2018-06-01 | View |
No matching devices.