ClearanceBrief
510(k) K802343 ยท JHJ Agglutination Method, Human Chorionic Gonadotropin

PREGNA B-ANTI HUMAN CHORIONIC GONADOTRO

ApplicantIntl. Diagnostic, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 10, 1980
ReceivedSep 26, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802343

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.