Pfm Medical, Inc.
FDA 510(k) & PMA Approved Devices — 19 products
Advertisement
Total Devices19
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K242763 | JetCan® Pro Safety Huber Needle | FPA | 2025-05-02 | View |
| 510(k) | K241278 | ASEPT® Glide Peritoneal Drainage System | PNG | 2025-01-14 | View |
| 510(k) | K221779 | ASEPT Peritoneal Drainage System | PNG | 2023-05-02 | View |
| 510(k) | K213666 | NuCath Wedge Pressure Catheter | DQO | 2022-10-06 | View |
| 510(k) | K201137 | Asept Surgical Face Mask | FXX | 2020-08-19 | View |
| 510(k) | K192802 | primeMidline Catheters | PND | 2019-10-28 | View |
| 510(k) | K173114 | primeMidline Catheters | PND | 2018-03-07 | View |
| 510(k) | K122402 | LPP (LOW PROFILE PORT) | LJT | 2013-07-16 | View |
| 510(k) | K113354 | VETA PERITONEAL DIALYSIS CATHETER | FJS | 2012-03-13 | View |
| 510(k) | K110914 | TRIPLE LUMEN PFM PICC | LJS | 2011-09-21 | View |
| 510(k) | K093796 | ASEPT PERITONEAL DRAINAGE SYSTEM | PNG | 2010-02-26 | View |
| 510(k) | K093307 | ASEPT PLEURAL DRAINAGE SYSTEM | DWM | 2009-11-06 | View |
| 510(k) | K083873 | PICC (CT RATED AND NON-RATED) | LJS | 2009-03-19 | View |
| 510(k) | K072481 | JET PORT PLUS HP CATHETER SYSTEM | LJT | 2008-03-07 | View |
| 510(k) | K073210 | MODIFICATION TO: T-PORT HP INFUSION PORT | LJT | 2007-12-12 | View |
| 510(k) | K072391 | PFM PICC | LJS | 2007-11-19 | View |
| 510(k) | K071993 | T-PORT HP INFUSION PORT | LJT | 2007-10-17 | View |
| 510(k) | K071846 | MODIFICATION TO EZ HUBER SAFETY INFUSION SET | FPA | 2007-08-30 | View |
| 510(k) | K040533 | EZ HUBER SAFETY INFUSION SET | FPA | 2004-09-17 | View |
No matching devices.
Advertisement