Gds Technology, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gds Technology, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Gds Technology, LLC has 7 FDA 510(k) cleared medical devices. Based in Elkhart, US.
Historical record: 7 cleared submissions from 1988 to 2000. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Gds Technology, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gds Technology, LLC
7 devices
Cleared
Jan 14, 2000
HEMOSITE TEST SYSTEM
Hematology
43d
Cleared
Aug 20, 1999
CHOLESITE TEST SYSTEM
Chemistry
58d
Cleared
Aug 31, 1998
HEMOSITE TEST SYSTEM
Microbiology
340d
Cleared
Sep 17, 1997
GLUCOSITE TEST SYSTEM
Chemistry
173d
Cleared
Jul 01, 1991
KETOSITE(TM)/STAT-SITE(TM)/KETOSITE(TM) LOW-HI CON
Chemistry
69d
Cleared
Jun 24, 1988
GDS ENZYMATIC SALICYLATE REAGENT
Chemistry
39d
Cleared
May 27, 1988
GDS ENZYMATIC ACETAMINOPHEN REAGENT
Toxicology
87d