Seigla Medical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2025-04-04
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243691 | LiquID .051 LP Guide Catheter Extension | DQY | 2025-04-04 | View |
| 510(k) | K220691 | LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension | DQY | 2022-05-05 | View |
No matching devices.