ClearanceBrief
510(k) K153703 ยท DQY Catheter, Percutaneous

Guiding Catheter

ApplicantTexasmedical Technologies, Inc., El Paso TN, US
DecisionSubstantially Equivalent, May 12, 2016
ReceivedDec 23, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K153703

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.