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FDA 510(k) Applications Submitted by DI-CHEM, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171015
04/04/2017
Citryte
Di-Chem, Inc.
K202508
08/31/2020
Hemo-Lyte C Cartridge
Di-Chem, Inc.
K012328
07/23/2001
HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE POWDER
DI-CHEM, INC.
K012547
08/07/2001
HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION
DI-CHEM, INC.
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