FDA 510(k) Applications for Medical Device Product Code: NDZ (Assay, Nucleic Acid Amplification, Growth Identification, Mycobacterium Tuberculosis)

FDA 510(k) Applications for Medical Device Product Code "NDZ"
(Assay, Nucleic Acid Amplification, Growth Identification, Mycobacterium Tuberculosis)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K000884	BECTON DICKINSON BIOSCIENCES	BD PROBETEC ET MYCOBACTERIUM TUBERCULOSIS COMPLEX (CTB) CULTURE IDENTIFICATION ASSAY	01/19/2001