ClearanceBrief
510(k) K885030 ยท FPA Set, Administration, Intravascular

STANDARD ADMINISTRATION SETS

Applicant3M Company, St. Paul MN, US
DecisionSubstantially Equivalent, Jan 24, 1989
ReceivedDec 5, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K885030

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.