ClearanceBrief
510(k) K050046 ยท IPF Stimulator, Muscle, Powered

REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S

ApplicantCompex Technologies, Inc., New Brighton MN, US
DecisionSubstantially Equivalent, Apr 13, 2005
ReceivedJan 10, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050046

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.