ClearanceBrief
510(k) K042590 ยท EGJ Device, Iontophoresis, Other Uses

TRANSDERM IONTO SYSTEM, MK 2

ApplicantMattioli Engineering Corp., Beltsville MD, US
DecisionSubstantially Equivalent, Oct 14, 2004
ReceivedSep 23, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042590

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.