FDA 510(k) Applications Submitted by Sheina Rajkumar
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K233201 | 09/28/2023 | MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter) | Penumbra, Inc. |
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