FDA 510(k) Applications Submitted by Q'Apel
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190749 | 03/25/2019 | 087 Balloon Guide Catheter System | Q'Apel |
| K181000 | 04/16/2018 | SelectFlex 072 Neurovascular Access System | Q'Apel |
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