ClearanceBrief
510(k) K770717 ยท EGJ Device, Iontophoresis, Other Uses

IONTOPHORESIS SYSTEM MODULE, DM 500

ApplicantSorensen Research, Walker MI, US
DecisionSubstantially Equivalent, Aug 15, 1977
ReceivedApr 18, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770717

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.