ClearanceBrief
510(k) K863099 ยท JJK Oncometer, Plasma, For Clinical Use

ABBOTT TESTPACK (TM) ACUTE HEP A CONTROL KIT

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, Sep 16, 1986
ReceivedAug 13, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863099

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.