ClearanceBrief
510(k) K040100 ยท DQX Wire, Guide, Catheter

ARROW ECHOGENIC INTRODUCER NEEDLE

ApplicantArrow Intl., Inc., Reading PA, US
DecisionSubstantially Equivalent, Mar 1, 2004
ReceivedJan 20, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040100

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.