FDA product code MUL: Generator, Electrosurgical, Coagulation, Cancer
MUL is the FDA product code for generator, electrosurgical, coagulation, cancer. It is a Class II device, regulated under 21 CFR 878.4400 and reviewed by the General and Plastic Surgery panel. Devices under MUL reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Generator, Electrosurgical, Coagulation, Cancer |
| Device class | Class II |
| Regulation | 21 CFR 878.4400 |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | General, Plastic Surgery |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for MUL devices
openFDA lists no recalls for product code MUL.
Frequently asked questions
What is FDA product code MUL?
MUL is the FDA product code for generator, electrosurgical, coagulation, cancer. It is a Class II device, regulated under 21 CFR 878.4400 and reviewed by the General and Plastic Surgery panel.
What device class is MUL?
Class II, regulation 21 CFR 878.4400. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code MUL
- Run a recall and safety report across every MUL manufacturer
- Watch product code MUL 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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