ClearanceBrief
510(k) K955410 ยท FPA Set, Administration, Intravascular

SNAPDOSE DEVICE

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, May 6, 1996
ReceivedNov 27, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955410

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.