ClearanceBrief
510(k) K853635 ยท EGJ Device, Iontophoresis, Other Uses

SUBDERM TM

ApplicantGeneral Medical Co., Washington DC, US
DecisionSubstantially Equivalent, Dec 20, 1985
ReceivedAug 30, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853635

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.