ClearanceBrief
510(k) K970491 ยท EGJ Device, Iontophoresis, Other Uses

DUPEL II BUFFERED IONTOPHORESIS ELECTRODES

ApplicantEmpi, St. Paul MN, US
DecisionSubstantially Equivalent, May 30, 1997
ReceivedFeb 10, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970491

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.