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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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