Medical Device Manufacturer · US , Mchenry , IL

Clinical Data, Inc. - FDA 510(k) Cleared Devices

36 submissions · 36 cleared · Since 1982

Recent clearances: ENVOY 500 HDL, NANOPIA WIDE RANGE C-REACTIVE PROTEIN (CRP) REAGENT KIT, VITALAB IRON REAGENT

Total

Cleared

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.

510(k) submissions have been managed by Entela, Inc. as regulatory consultant.

Clinical Data, Inc. is one of 6901 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Clinical Data, Inc.

36 devices

1-12 of 36

NANOPIA WIDE RANGE C-REACTIVE PROTEIN (CRP) REAGENT KIT

VITALAB DIRECT BILIRUBIN REAGENT

K040631 · CIG

Chemistry · 8d

Cleared Mar 11, 2004

VITALAB AMYLASE REAGENT

K040534 · JFJ

Chemistry · 9d

Cleared Mar 10, 2004

VITALAB TRIGLYCERIDES REAGENT AND VITALAB CALIBRATOR

K034000 · CDT

Chemistry · 77d

Cleared Mar 08, 2004

VITALAB URIC ACID REAGENT

K040467 · KNK

Chemistry · 13d

Cleared Mar 08, 2004

VITALAB MAGNESIUM REAGENT

K040508 · JGJ

Chemistry · 10d

Cleared Nov 03, 2003

ATAC HEMOGLOBIN A1C REAGENT KIT

K031042 · LCP

Chemistry · 216d

Cleared Jul 15, 2003

ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR

K031044 · KNK

Toxicology · 105d

Cleared Jan 06, 1987

DISPOSABLE ECG MONITORING ELECTRODE

K863904 · DRX

Cardiovascular · 91d

Cleared Jan 22, 1986

DETERMINATION OF GENTAMICIN

K860045 · LCD

Toxicology · 16d

Clinical Data, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Clinical Data, Inc.

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