ClearanceBrief
510(k) K080178 ยท MGZ Valvulotome

VALVULOTOME BY KOVEN

ApplicantKoven Technology, Inc., Houston TX, US
DecisionSubstantially Equivalent, Jul 28, 2008
ReceivedJan 24, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K080178

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.