ClearanceBrief
510(k) K902858 ยท FPA Set, Administration, Intravascular

AVI MODEL 4206 MANIFOLD CHECKVALVE IV ADMIN. SET

Applicant3M Avi, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Dec 14, 1990
ReceivedJun 29, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902858

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.