FDA 510(k) Applications Submitted by Lori Grace
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| DEN240048 | 09/20/2024 | Spur Peripheral Retrievable Stent System | Reflow Medical, Inc. |
| K233350 | 09/29/2023 | SINC Support Catheter | Reflow Medical, Inc. |
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