FDA 510(k) Applications Submitted by STANDARD DIAGNOSTICS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K031798 06/10/2003 GOOD MORNING TEST STANDARD DIAGNOSTICS, INC.
K100398 02/16/2010 SMARTLINK GOLD BLOOD GLUCOSE MONITORING SYSTEM STANDARD DIAGNOSTICS, INC.
K082683 09/15/2008 SD CHECK GOLD STANDARD DIAGNOSTICS, INC.


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