Clinical Data, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clinical Data, Inc. - FDA 510(k) Cleared Devices
36
Total
36
Cleared
0
Denied
Clinical Data, Inc. has 36 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 36 cleared submissions from 1982 to 2007. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Clinical Data, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Clinical Data, Inc.
36 devices
Cleared
Dec 20, 2007
ENVOY 500 HDL
Chemistry
182d
Cleared
Feb 09, 2006
NANOPIA WIDE RANGE C-REACTIVE PROTEIN (CRP) REAGENT KIT
Chemistry
141d
Cleared
May 21, 2004
VITALAB IRON REAGENT
Chemistry
150d
Cleared
Mar 18, 2004
VITALAB DIRECT BILIRUBIN REAGENT
Chemistry
8d
Cleared
Mar 11, 2004
VITALAB AMYLASE REAGENT
Chemistry
9d
Cleared
Mar 10, 2004
VITALAB TRIGLYCERIDES REAGENT AND VITALAB CALIBRATOR
Chemistry
77d
Cleared
Mar 08, 2004
VITALAB URIC ACID REAGENT
Chemistry
13d
Cleared
Mar 08, 2004
VITALAB MAGNESIUM REAGENT
Chemistry
10d
Cleared
Nov 03, 2003
ATAC HEMOGLOBIN A1C REAGENT KIT
Chemistry
216d
Cleared
Jul 15, 2003
ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR
Toxicology
105d
Cleared
Jan 06, 1987
DISPOSABLE ECG MONITORING ELECTRODE
Cardiovascular
91d
Cleared
Jan 22, 1986
DETERMINATION OF GENTAMICIN
Toxicology
16d