ClearanceBrief
510(k) K120129 ยท DQY Catheter, Percutaneous

MANTARAY CATHETER

ApplicantBridgepoint Medical, Plymouth MN, US
DecisionSubstantially Equivalent, Feb 3, 2012
ReceivedJan 17, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120129

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.