ClearanceBrief
510(k) K031359 ยท PJE Blood/Plasma Collection Device For Dna Testing

S-MONOVETTE EDTA K2-GEL

ApplicantSarstedt, Inc., Newton NC, US
DecisionSubstantially Equivalent, Sep 12, 2003
ReceivedApr 30, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031359

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.