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Megapulse III/OmniSWD

ACCELERATED CARE PLUS CORP · Model 1903030 · UDI-DI 00858703006085

IMJ Prescription
1
510(k) clearances
25
Adverse events
1
Recalls
16
Facilities

Description

Shortwave Diathermy for the use of applying therapeutic deep heat

Recalls

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

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.