ClearanceBrief
510(k) K891005 ยท FPK Tubing, Fluid Delivery

INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050

Applicant3M Company, St. Paul MN, US
DecisionSubstantially Equivalent, May 11, 1989
ReceivedFeb 28, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K891005

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.