FDA product code LOC: System, Rf/Microwave Hyperthermia, Cancer Treatment
LOC is the FDA product code for system, rf/microwave hyperthermia, cancer treatment. It is a Class III device, reviewed by the Radiology panel. Devices under LOC 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, Rf/Microwave Hyperthermia, Cancer Treatment |
| Device class | Class III |
| Review panel | RA — Radiology |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for LOC devices
openFDA lists no recalls for product code LOC.
Frequently asked questions
What is FDA product code LOC?
LOC is the FDA product code for system, rf/microwave hyperthermia, cancer treatment. It is a Class III device, reviewed by the Radiology panel.
What device class is LOC?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code LOC
- Run a recall and safety report across every LOC manufacturer
- Watch product code LOC 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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