ClearanceBrief
510(k) K902822 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

MEDICAL DESIGNS, INC., SPECTRUM II TENS DEVICE

ApplicantMedical Design & Manufacturing Corp., Westerville OH, US
DecisionSubstantially Equivalent, Dec 19, 1990
ReceivedJun 27, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902822

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.