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
K891167 DIAGNOSTIC PRODUCTS CORP. COAT-A-COUNT(TM) LSD RADIOIMMUNOASSAY KIT 05/03/1989
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
K860525 ROCHE DIAGNOSTIC SYSTEMS, INC. ABUSCREEN RADIOIMMUNOASSAY FOR LSD W/ REF STANDARD 04/11/1986
K874270 ROCHE DIAGNOSTIC SYSTEMS, INC. REVISED LABELING FOR LSD TEST KIT 11/13/1987
K954073 SOLARCARE TECHNOLOGIES CORP,INC. STC DIAGNOSTICS LSD MICRO-PLATE EIA 11/29/1995


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