ClearanceBrief
510(k) K993081 ยท EGJ Device, Iontophoresis, Other Uses

IO-DRIVE

ApplicantSelectivemed Components, Inc., Mount Vernon OH, US
DecisionSubstantially Equivalent, Mar 3, 2000
ReceivedSep 15, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993081

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.