ClearanceBrief
510(k) K122940 ยท DQY Catheter, Percutaneous

ADVANCE MICRO 14 ULTRA LOW PROFILE BALLOON DILATATION CATHETER MODEL PTA3

ApplicantCook, Inc., Bloomington IN, US
DecisionSubstantially Equivalent, Mar 19, 2013
ReceivedSep 24, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122940

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.