ClearanceBrief
510(k) K972969 ยท GIO Tube, Collection, Capillary Blood

QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM

ApplicantInnovative Medical Technologies, Inc., Lenexa KS, US
DecisionSubstantially Equivalent, Sep 22, 1997
ReceivedAug 11, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972969

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.