ClearanceBrief
510(k) K850507 ยท FPA Set, Administration, Intravascular

CRITIKON I.V. ADMINISTRAION SET

ApplicantCritikon Company, LLC, Tampa FL, US
DecisionSubstantially Equivalent, Mar 7, 1985
ReceivedFeb 8, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850507

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.