ClearanceBrief
510(k) K900657 ยท DQY Catheter, Percutaneous

UNIVERSAL DELIVERY SYSTEM CATHETER

ApplicantMicrovena Corp., Findley MN, US
DecisionSubstantially Equivalent, May 9, 1990
ReceivedFeb 9, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900657

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.