FDA 510(k) Applications for Medical Device Product Code "MJD"
(Culture Media, Antimycobacteria, Susceptibility Test)

FDA 510(k) Number Applicant Device Name Decision Date
K823859 GIBCO LABORATORIES LIFE TECHNOLOGIES, INC. MIDDLEBROOK 7H10 AGAR BASE-LOWPH 03/08/1983
K840981 REMEL CO. NIACIN REAGENT STRIP 03/23/1984
K920143 REMEL CO. TB SUSCEPTIBILITY QUADS I AND II 06/09/1992


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