Neurologica Corporation, A Subsidiary of Samsung
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2025-03-14
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K242811 | BodyTom 64 | JAK | 2025-03-14 | View |
| 510(k) | K223447 | OmniTom Elite | JAK | 2023-06-01 | View |
No matching devices.