ClearanceBrief
510(k) K094019 ยท DQY Catheter, Percutaneous

GLIDER PTA BALLOON CATHETER

ApplicantTrireme Medical, Inc., Pleasanton CA, US
DecisionSubstantially Equivalent, Feb 12, 2010
ReceivedDec 29, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K094019

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.