ClearanceBrief
510(k) K913803 ยท DWX Stripper, Artery, Intraluminal

INTRALUMINAL ARTERY STRIPPER

ApplicantOmni-Tract Surgical, Div. Minn. Scientific, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Apr 24, 1992
ReceivedAug 26, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913803

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.