ClearanceBrief
510(k) K072256 ยท PFW Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat

HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED STIMULATION SYSTEM WITH OPTIONAL HANDS-FREE OPERATION, MODEL

ApplicantHill Laboratories Co., Frazer PA, US
DecisionSubstantially Equivalent, Mar 12, 2008
ReceivedAug 13, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072256

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.