ClearanceBrief
510(k) K780310 ยท

DERMATRON IONTOPHORESIS DEVICE

ApplicantMotion Control, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jul 31, 1978
ReceivedFeb 21, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780310

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.