ClearanceBrief
510(k) K963693 ยท CEP Radioimmunoassay, Luteinizing Hormone

OVUSIGN - ONE-STEP HOME OVULATION PREDICTOR TEST

ApplicantPrinceton BioMeditech Corp., Princeton NJ, US
DecisionSubstantially Equivalent, Nov 29, 1996
ReceivedSep 16, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963693

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.