ClearanceBrief
510(k) K093050 ยท DQY Catheter, Percutaneous

ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520

ApplicantArrow Intl., Inc., Reading PA, US
DecisionSubstantially Equivalent, Dec 18, 2009
ReceivedSep 30, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093050

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.