ClearanceBrief
510(k) K854804 ยท FPA Set, Administration, Intravascular

MULTIPLE I.V. SETS

ApplicantC. B. Dumont Company, Inc., Newport RI, US
DecisionSubstantially Equivalent, Feb 12, 1986
ReceivedDec 2, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854804

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.