ClearanceBrief
510(k) K032003 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

PREMIER PLUS

ApplicantAmerican Imex, Irvine CA, US
DecisionSubstantially Equivalent, Jan 7, 2004
ReceivedJun 27, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032003

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.