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FDA 510(k) Applications Submitted by Anush Puvvada
FDA 510(k) Number
Submission Date
Device Name
Applicant
K202251
08/10/2020
Penumbra System (Penumbra JET 7 Reperfusion Catheter with Xtra Flex Technology; Penumbra JET 7MAX)
Penumbra, Inc.
K192955
10/21/2019
Penumbra LP Coil System
Penumbra, Inc.
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