FDA 510(k) Applications Submitted by Ryan Rivera
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230726 | 03/16/2023 | CEREGLIDE 92 Intermediate Catheter | Cerenovus, Inc. |
| K233988 | 12/18/2023 | Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set | Cerenovus, Inc. |
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