ClearanceBrief
510(k) K991751 ยท DKE Reagents, Test, Tetrahydrocannabinol

STATUS CUP ACCUSIGN CUP

ApplicantPrinceton BioMeditech Corp., Monmouth Junction NJ, US
DecisionSubstantially Equivalent, Jun 18, 1999
ReceivedMay 24, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K991751

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.