ClearanceBrief
510(k) K061522 ยท EGJ Device, Iontophoresis, Other Uses

TRIVARION BUFFERED IONTOPHORESIS ELECTRODE SYSTEM

ApplicantActivatek, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Aug 1, 2006
ReceivedJun 2, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061522

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.