ClearanceBrief
510(k) K030395 ยท EGJ Device, Iontophoresis, Other Uses

EMPI ACTION PATCH IONTOPHORESIS SYSTEM

ApplicantEmpi, Washington DC, US
DecisionSubstantially Equivalent, Apr 8, 2003
ReceivedFeb 5, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030395

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.