ClearanceBrief
510(k) K913643 ยท BYZ Trap, Sterile Specimen

MUCOUS SPECIMEN TRAP

ApplicantMedical Device Inspection Co., Inc., Great Neck NY, US
DecisionSubstantially Equivalent, Oct 10, 1991
ReceivedAug 14, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913643

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.