ClearanceBrief
510(k) K862273 ยท LDR Controller, Infusion, Intravascular, Electronic

BETAFLO 2000

ApplicantBetaflo, Inc., Menlo Park CA, US
DecisionSubstantially Equivalent, Jul 18, 1986
ReceivedJun 16, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862273

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.