FDA 510(k) Applications for Medical Device Product Code: LJP (Antiserum, Fluorescent, Chlamydia Trachomatis)

FDA 510(k) Applications for Medical Device Product Code "LJP"
(Antiserum, Fluorescent, Chlamydia Trachomatis)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K063675	DIAGNOSTIC HYBRIDS, INC.	DIAGNOSTIC HYBRIDS' D3 DFA CHLAMYDIAE CULTURE CONFIRMATION KIT	09/24/2007