FDA product code MVG: System, Laser, Fiber Optic, Photodynamic Therapy
MVG is the FDA product code for system, laser, fiber optic, photodynamic therapy. It is a Class III device, reviewed by the General and Plastic Surgery panel. Devices under MVG reach the market by PMA; FDA lists no cleared 510(k)s for it. 2 PMA applications cite this product code.
Classification
| Field | Value |
|---|---|
| Device name | System, Laser, Fiber Optic, Photodynamic Therapy |
| Device class | Class III |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for MVG devices
openFDA lists no recalls for product code MVG.
Frequently asked questions
What is FDA product code MVG?
MVG is the FDA product code for system, laser, fiber optic, photodynamic therapy. It is a Class III device, reviewed by the General and Plastic Surgery panel.
What device class is MVG?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MVG
- Run a recall and safety report across every MVG manufacturer
- Watch product code MVG 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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