Q'Apel
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| 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.
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