FDA 510(k) Applications for Medical Device Product Code: LJK (Antisera, If, Toxoplasma Gondii)

FDA 510(k) Applications for Medical Device Product Code "LJK"
(Antisera, If, Toxoplasma Gondii)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K974261	BOSTON BIOMEDICA, INC.	ACCURUN 135 TOXOPLASMA IGG POSITIVE CONTROL	12/11/1997