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FDA 510(k) Applications Submitted by CHARLES PENNINGTON
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
K082499
08/29/2008
C. DIFF QUIK CHEK COMPLETE
TECHLAB, INC.
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