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FDA 510(k) Applications Submitted by CHRONIMED, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010039
01/05/2001
QUICKTEK BLOOD GLUCOSE SYSTEM, QUICKTEK BLOOD GLUCOSE METER, QUICKTEK BLOOD GLUCOSE STRIPS, QUICKTEK CONTROL SOLUTION
CHRONIMED, INC.
K980573
02/17/1998
SENSOREX BLOOD GLUCOSE MONITORING SYSTEM
CHRONIMED, INC.
K963544
09/04/1996
SUPREME II METER
CHRONIMED, INC.
K983432
09/29/1998
SUPREME II CONTROL SOLUTIONS
CHRONIMED, INC.
K981555
05/01/1998
DIASCREEN REAGENT STRIPS
CHRONIMED, INC.
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