ClearanceBrief
510(k) K110813 ยท DQY Catheter, Percutaneous

HEADWAY 27 MICROCATHETER

ApplicantMicroVention, Inc., Tistin CA, US
DecisionSubstantially Equivalent, Aug 5, 2011
ReceivedMar 24, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K110813

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.