ClearanceBrief
510(k) K912860 ยท FPA Set, Administration, Intravascular

INTRAVASCULAR ADMINISTRATION SETS

ApplicantPacific Device, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Aug 28, 1991
ReceivedJun 27, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912860

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.