ClearanceBrief
510(k) K070541 ยท ILX Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat

IVIVI SOFPULSE, MODELS 912-M10, ROMA3 AND TORINO II

ApplicantIvivi Technologies, Inc., Northvale NJ, US
DecisionSubstantially Equivalent, Dec 11, 2008
ReceivedFeb 26, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070541

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.