ClearanceBrief
510(k) K972075 ยท PJE Blood/Plasma Collection Device For Dna Testing

VACUTAINER BRAND PPT PLASMA PREPARATION TUBE

ApplicantBecton Dickinson Vacutainer Systems, Franklin Lake NJ, US
DecisionSubstantially Equivalent, Feb 24, 1998
ReceivedJun 3, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972075

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.