FDA 510(k) Applications Submitted by Apurva Gokhale
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K250542 | 02/24/2025 | AC3Ö RangeÖ Intra-Aortic Balloon Pump | Arrow International LLC |
| K200634 | 03/10/2020 | Arrow FiberOptix Intra-Aortic Balloon Catheter Kit | Arrow International Inc. |
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