U. S. Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
U. S. Diagnostics, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
U. S. Diagnostics, Inc. has 22 FDA 510(k) cleared medical devices. Based in San Luis Obispo, US.
Historical record: 22 cleared submissions from 1986 to 2011. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by U. S. Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - U. S. Diagnostics, Inc.
22 devices
Cleared
Sep 21, 2011
EASYGLUCO PLUS BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
218d
Cleared
Feb 20, 2009
G5 INFINITY BLODO GLUCOSE MONITORING SYSTEM WITH MODEL IGM, 0024A
Chemistry
199d
Cleared
Jan 12, 2007
EASYGLUCO, MODEL IGM-0002 G2
Chemistry
233d
Cleared
Apr 14, 2006
G4, MODEL IGM-0004
Chemistry
297d
Cleared
Apr 20, 1987
PROTHROMBIN TIME TEST
Hematology
69d
Cleared
Apr 20, 1987
COAGULATION CONTROL, LEVEL I
Hematology
60d
Cleared
Apr 20, 1987
COAGULATION CONTROL, LEVEL II
Hematology
60d
Cleared
Apr 20, 1987
COAGULATION CONTROL, LEVEL III
Hematology
60d
Cleared
Apr 15, 1987
CYANMETHEMOGLOBIN STANDARD
Hematology
15d
Cleared
Apr 13, 1987
U.S. DIAGNOSTICS LIQUID LD ISOENZYME CONTROL
Chemistry
47d
Cleared
Apr 13, 1987
U.S. DIAGNOSTICS LIQUID CK ISOENZYME CONTROL
Chemistry
47d
Cleared
Apr 06, 1987
LIQUID CHEMISTRY CONTROL, LEVEL II
Chemistry
46d