Q'Apel
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2019-07-15
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K190749 | 087 Balloon Guide Catheter System | DQY | 2019-07-15 | View |
| 510(k) | K181000 | SelectFlex 072 Neurovascular Access System | DQY | 2018-09-13 | View |
No matching devices.