ClearanceBrief
510(k) K780526 ยท GMD Antisera, Latex Agglutination, Cryptococcus Neoformans

CRYPTOCOCCAL ANTIGEN LATEX AGG. SYSTEM

ApplicantI M, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 28, 1978
ReceivedMar 31, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780526

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.