FDA 510(k) Applications for Medical Device Product Code "DEG"
(Lactoferrin, Antigen, Antiserum, Control)

FDA 510(k) Number Applicant Device Name Decision Date
K071712 TECHLAB INC., CORPORATE RESEARCH CENTER LEUKO EZ VUE 12/04/2007
K011396 TECHLAB, INC. IBD-CHEK 06/18/2001
K030704 TECHLAB, INC. IBD-QUIK CHEK 04/21/2003
K042071 TECHLAB, INC. IBD-SCAN 10/20/2004


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