FDA 510(k) Applications for Medical Device Product Code "DLB"
(Radioimmunoassay, Lsd (125-I))

FDA 510(k) Number Applicant Device Name Decision Date
K955448 BEHRING DIAGNOSTICS, INC. EMIT II LSD ASSAY, EMIT LSD CALIBRATORS & EMIT LSD CONTROLS 02/23/1996
K955814 MICROGENICS CORP. CEDIA DAU LSD ASSAY 02/09/1996
K961436 ROCHE DIAGNOSTIC SYSTEMS, INC. ABUSCREEN ONLINE LSD REAGENT (90 ML TEST KIT) 06/21/1996


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