FDA 510(k) Applications Submitted by TECHLAB INC., CORPORATE RESEARCH CENTER

FDA 510(k) Number Submission Date Device Name Applicant
K071711 06/22/2007 ASCA-CHEK TECHLAB INC., CORPORATE RESEARCH CENTER
K071712 06/22/2007 LEUKO EZ VUE TECHLAB INC., CORPORATE RESEARCH CENTER
K121364 05/07/2012 SHIGA TOXIN QUIK CHEK TECHLAB INC., CORPORATE RESEARCH CENTER
K121411 05/11/2012 SHIGA TOXIN CHEK TECHLAB INC., CORPORATE RESEARCH CENTER
K103673 12/16/2010 GIARDIA/ CRYPTOSPORIDIUM QUIK CHEK TECHLAB INC., CORPORATE RESEARCH CENTER


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