Q'Apel
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| 087 Balloon Guide Catheter System (K190749) | Q'Apel | 2019-07-15 |
| SelectFlex 072 Neurovascular Access System (K181000) | Q'Apel | 2018-09-13 |
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Every clearance here is in the API, with alerts when new ones post.