ClearanceBrief
510(k) K894851 ยท GIO Tube, Collection, Capillary Blood

TRU-TRAX

ApplicantHumagen, Inc., Charlottesville VA, US
DecisionSubstantially Equivalent, Sep 29, 1989
ReceivedJul 31, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894851

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.