ClearanceBrief
510(k) K831366 ยท JHJ Agglutination Method, Human Chorionic Gonadotropin

TESTCORP PREG

ApplicantCatheter Technology Corp., Walker MI, US
DecisionSubstantially Equivalent, Jun 2, 1983
ReceivedApr 26, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831366

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.