ClearanceBrief
510(k) K982141 ยท DXE Catheter, Embolectomy

ARROW 5FX60CM BALLOON EMBOLECTOMY CATHETER, MODEL # EM-56025

ApplicantArrow Intl., Inc., Reading PA, US
DecisionSubstantially Equivalent, Aug 31, 1998
ReceivedJun 17, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982141

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.