FDA 510(k) Applications for Medical Device Product Code: LTX (Discs, Elution)

FDA 510(k) Applications for Medical Device Product Code "LTX"
(Discs, Elution)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K992993	AB BIODISK	ETEST FOR QUINUPRISTIN/DALFOPRISTIN	11/16/1999
K002139	AB BIODISK	ETEST LINEZOLID	11/08/2000