ClearanceBrief
510(k) K770467 ยท

IN VITRO DIAGNOSTIC TEST

ApplicantHoffmann-La Roche, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 27, 1977
ReceivedMar 10, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770467

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.