FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VITALAB URIC ACID REAGENT

K Number: K040467 · Decision Mar 8, 2004
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
117
Applicant Total
36
Review Days
13

Basic Information

Device Name
VITALAB URIC ACID REAGENT
K Number
K040467
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1775
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CLINICAL DATA, INC.
Date Received
February 24, 2004
Decision Date
March 8, 2004
Product Code
KNK
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNK Acid, Uric, Uricase (Colorimetric)

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Other Clearances by CLINICAL DATA, INC.

K Number Device Name
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K052591 NANOPIA WIDE RANGE C-REACTIVE PROTEIN (CRP) REAGENT KIT
K033983 VITALAB IRON REAGENT
K040631 VITALAB DIRECT BILIRUBIN REAGENT
K040534 VITALAB AMYLASE REAGENT
K034000 VITALAB TRIGLYCERIDES REAGENT AND VITALAB CALIBRATOR
K040508 VITALAB MAGNESIUM REAGENT
K031042 ATAC HEMOGLOBIN A1C REAGENT KIT
K031044 ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR
K863904 DISPOSABLE ECG MONITORING ELECTRODE
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