Medical Device Manufacturer · US , Mchenry , IL

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

36 submissions · 36 cleared · Since 1982

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.

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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