ClearanceBrief
510(k) K831950 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

PULSAR #B SINGLE CHANNEL TENS-PULSAR D

ApplicantSpembly Medical , Ltd., Walker MI, US
DecisionSubstantially Equivalent, Aug 1, 1983
ReceivedJun 15, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831950

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.