Worthington Diagnostic Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Worthington Diagnostic Systems - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Worthington Diagnostic Systems has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1979 to 1984. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Worthington Diagnostic Systems Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Worthington Diagnostic Systems
19 devices
Cleared
Jan 04, 1984
COMPUR* M1000 HEMOGLOBIN & ERYTHROCYTE
Hematology
76d
Cleared
Oct 14, 1983
EASYTOUCH TROMBOPLASTIN REAGENT
Chemistry
84d
Cleared
Oct 14, 1983
COMPUR* EASYTOUCH TOTAL BILIRUBIN
Chemistry
60d
Cleared
Oct 14, 1983
EASYTOUCH BUN REAGENT SET
Chemistry
60d
Cleared
Oct 14, 1983
COMPUR* EASY TOUCH URIC ACID REAGENT
Chemistry
59d
Cleared
Sep 26, 1983
EASYTOUCH HEMOGLOBIN REAGENT
Chemistry
42d
Cleared
Sep 12, 1983
EASYTOUCH TRIGLYCERIDES REAGENT SET
Chemistry
52d
Cleared
Jun 17, 1983
DEMAND ANALYZER SYSTEM
Chemistry
39d
Cleared
Jun 08, 1983
COMPUR* M1100 HEMATRCRIT SYSTEM
Hematology
47d
Cleared
Jun 02, 1983
COMPUR EASY TOUCH CHEMISTRY ANALYZER-
Chemistry
48d
Cleared
Apr 27, 1983
TIA-IGG REAGENT & CALIBRATOR SETS
Immunology
22d
Cleared
Apr 27, 1983
TIA-IGA REAGENT & CALIBRATOR SETS
Immunology
22d