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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