ClearanceBrief
510(k) K970080 ยท MCW Catheter, Peripheral, Atherectomy

ARROW-TREROTOLA PTD CATHETER

ApplicantArrow Intl., Inc., Reading PA, US
DecisionSubstantially Equivalent, Jul 25, 1997
ReceivedJan 9, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970080

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.