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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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