FDA 510(k) Applications Submitted by Penumbra, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221822 | 06/23/2022 | BENCHMARK BMX81 Access System | Penumbra, Inc |
| K192981 | 10/24/2019 | Indigo System Aspiration Catheter 12, Indigo Aspiration System Separator 12 | Penumbra, Inc |
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