FDA 510(k) Applications for Medical Device Product Code: LQH (Dna-Reagents, Legionella)

FDA 510(k) Applications for Medical Device Product Code "LQH"
(Dna-Reagents, Legionella)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K033861	BECTON, DICKINSON & CO.	BD PROBETEC ET LEGIONELLA PNEUMOPHILA (LP) AMPLIFIED DNA ASSAY	03/09/2004