FDA product code MVF: System, Laser, Photodynamic Therapy
MVF is the FDA product code for system, laser, photodynamic therapy. It is a Class III device, reviewed by the General and Plastic Surgery panel. Devices under MVF reach the market by PMA; FDA lists no cleared 510(k)s for it. 8 PMA applications cite this product code.
Classification
| Field | Value |
|---|---|
| Device name | System, Laser, Photodynamic Therapy |
| Device class | Class III |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for MVF devices
openFDA lists no recalls for product code MVF.
Frequently asked questions
What is FDA product code MVF?
MVF is the FDA product code for system, laser, photodynamic therapy. It is a Class III device, reviewed by the General and Plastic Surgery panel.
What device class is MVF?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MVF
- Run a recall and safety report across every MVF manufacturer
- Watch product code MVF for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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