ClearanceBrief
510(k) K031329 ยท IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)

ApplicantDynatronics Corp., Salt Lake City UT, US
DecisionSubstantially Equivalent, Oct 22, 2003
ReceivedApr 28, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031329

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.