FDA Device Intelligence
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Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

FDA product code IMJ · Class 2 · Physical Medicine

21
Registered devices
25
Adverse events
1
Recalls
45
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-08-21DJO, LLCOverheating and burning of the wire insulation inside the applicator.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.