ClearanceBrief
510(k) K924558 ยท DQX Wire, Guide, Catheter

ARROW BLOOD CONTAINMENT DEVICE

ApplicantArrow Intl., Inc., Reading PA, US
DecisionSubstantially Equivalent, Aug 19, 1993
ReceivedSep 9, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924558

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.