ClearanceBrief
510(k) K782063 ยท JHJ Agglutination Method, Human Chorionic Gonadotropin

PREGNANCY, SENSIDEX TUBE TEST

ApplicantOrtho Diagnostics, Inc., Walker MI, US
DecisionSubstantially Equivalent, Apr 4, 1979
ReceivedDec 11, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782063

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.