ClearanceBrief
510(k) K913601 ยท EGJ Device, Iontophoresis, Other Uses

MICROPHOR

ApplicantLife-Tech Intl., Inc., Houston TX, US
DecisionSubstantially Equivalent, Jul 15, 1994
ReceivedAug 13, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913601

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.