ClearanceBrief
510(k) K120881 ยท DQX Wire, Guide, Catheter

MANTARAY GUIDEWIRES

ApplicantBridgepoint Medical, Plymouth MN, US
DecisionSubstantially Equivalent, Apr 18, 2012
ReceivedMar 23, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120881

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.