FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

QUANTIMETRIX BIURET SERUM TOTAL PROTEIN ASSAY KIT

K Number: K853930 · Decision Dec 10, 1985
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
115
Applicant Total
38
Review Days
77

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Basic Information

Device Name
QUANTIMETRIX BIURET SERUM TOTAL PROTEIN ASSAY KIT
K Number
K853930
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1635
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Quantimetrix Corp.
Date Received
September 24, 1985
Decision Date
December 10, 1985
Product Code
CEK
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CEK Biuret (Colorimetric), Total Protein

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K032791 GLYCOHEMOSURE HBA1C CONTROL
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