FDA product code MWD: Electrosurgical, Radio Frequency, Refractive Correction
MWD is the FDA product code for electrosurgical, radio frequency, refractive correction. It is a Class III device, reviewed by the Ophthalmic panel. Devices under MWD reach the market by PMA; FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code.
Classification
| Field | Value |
|---|---|
| Device name | Electrosurgical, Radio Frequency, Refractive Correction |
| Device class | Class III |
| Review panel | OP — Ophthalmic |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for MWD devices
openFDA lists no recalls for product code MWD.
Frequently asked questions
What is FDA product code MWD?
MWD is the FDA product code for electrosurgical, radio frequency, refractive correction. It is a Class III device, reviewed by the Ophthalmic panel.
What device class is MWD?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MWD
- Run a recall and safety report across every MWD manufacturer
- Watch product code MWD 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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