ClearanceBrief
510(k) K110055 ยท DQY Catheter, Percutaneous

REVERSE MEDICAL REFLEX GUIDE CATHETER

ApplicantReverse Medical Corporation, Irvine CA, US
DecisionSubstantially Equivalent, Apr 5, 2011
ReceivedJan 10, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K110055

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.