FDA 510(k) Applications Submitted by PFM Medical, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221779 | 06/21/2022 | ASEPT Peritoneal Drainage System | PFM Medical, Inc. |
| K173114 | 09/29/2017 | primeMidline Catheters | PFM Medical, Inc. |
| K213666 | 11/22/2021 | NuCath Wedge Pressure Catheter | PFM Medical, Inc. |
| K192802 | 09/30/2019 | primeMidline Catheters | PFM Medical, Inc. |
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