Home › Device types › NMF
Clamp, Vascular, Reprocessed
FDA product code NMF · Class 2 · Cardiovascular
2
Registered devices
30
Adverse events
2
Recalls
3
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-06-23 | Ascent Healthcare Solutions, Inc. | The FemoStop Devices may fail to inflate or hold pressure. A separation between the dome and arch base prevents the device from maintaining pressure when infla |
| 2008-08-08 | Sterilmed Inc | SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted becau |
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