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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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