ClearanceBrief
510(k) K841853 ยท JHJ Agglutination Method, Human Chorionic Gonadotropin

PREG-BETA ONE HOUR TUBE TEST

ApplicantIntl. Diagnostic, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 22, 1984
ReceivedMay 3, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841853

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.