ClearanceBrief
510(k) K062885 ยท DQY Catheter, Percutaneous

STRIDE MICROCATHETER

ApplicantAsahi Intecc Co., Ltd., Newport Beach CA, US
DecisionSubstantially Equivalent, Jun 13, 2007
ReceivedSep 26, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062885

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.