ClearanceBrief
510(k) K140034 ยท DQY Catheter, Percutaneous

SUREFIRE GUIDING CATHETER

ApplicantSurefire Medical, Inc., Westminster CO, US
DecisionSubstantially Equivalent, Feb 26, 2014
ReceivedJan 7, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140034

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.