FDA 510(k) Applications for Medical Device Product Code "DFK"
(Igg (Fab Fragment Specific), Antigen, Antiserum, Control)

FDA 510(k) Number Applicant Device Name Decision Date
K771243 KENT LABORATORIES, INC. ANTISERA TO HUMAN FAB FRAGMENT 08/03/1977
K790711 KENT LABORATORIES, INC. ANTISERA TO HUMAN FRAGMENT 09/04/1979
K770670 KENT LABORATORIES, INC. FLOR. CONJUG. HUMAN FAB FRAGMENT 04/28/1977


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