FDA 510(k) Applications Submitted by Perfuze Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231802 | 06/20/2023 | Millipede 088 Access Catheter | Perfuze Ltd. |
| K214048 | 12/27/2021 | Millipede 088 Access Catheter | Perfuze Ltd. |
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