ClearanceBrief
510(k) K935811 ยท FPA Set, Administration, Intravascular

BOLUS DISPENSER

ApplicantI-Flow Corp., Irvine CA, US
DecisionSubstantially Equivalent, Jan 20, 1995
ReceivedDec 2, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935811

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.