ClearanceBrief
510(k) K961049 ยท FPA Set, Administration, Intravascular

FLEX NEEDLE

ApplicantLighthouse Medical, Inc., Waltham MA, US
DecisionSubstantially Equivalent, Sep 18, 1996
ReceivedMar 15, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961049

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.