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

QUANTIMETRIX BLOOD GLUCOSE CONTROLS

K Number: K932623 · Decision Dec 9, 1993
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
301
Applicant Total
38
Review Days
191

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Basic Information

Device Name
QUANTIMETRIX BLOOD GLUCOSE CONTROLS
K Number
K932623
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Quantimetrix Corp.
Date Received
June 1, 1993
Decision Date
December 9, 1993
Product Code
JIX
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
JIX Calibrator, Multi-Analyte Mixture

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K062751 MODIFICATION TO QUANTIMETRIX CARDIASURE CARDIAC MARKER
K060417 MODIFICATION TO QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL
K032791 GLYCOHEMOSURE HBA1C CONTROL
K030826 PRECISET DAT AMPHETAMINE
K021393 PRECISET DAT PLUS
K013662 MODIFICATION TO LIPOPRINT SYSTEM, LDL SUBFRACTIONS
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