FDA 510(k) Applications Submitted by Shalin Parikh
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230156 | 01/19/2023 | 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter | Medtronic Vascular |
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