Di-Chem, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Di-Chem, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Last cleared in 2022. Active since 1982. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Di-Chem, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Di-Chem, Inc.
6 devices
Cleared
Aug 12, 2022
Hemo-Lyte C Cartridge
Gastroenterology & Urology
711d
Cleared
Oct 13, 2017
Citryte
Gastroenterology & Urology
192d
Cleared
Jan 18, 2002
HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE POWDER
Gastroenterology & Urology
179d
Cleared
Jan 18, 2002
HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION
Gastroenterology & Urology
164d
Cleared
Apr 09, 1991
FORMASURE TEST REAGENT
Gastroenterology & Urology
140d
Cleared
Nov 17, 1982
DIALYSATE ADDITIVES-POWDER/LIQUID
Hematology
28d