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

QUANTIMETRIX URINALYSIS MICROSCOPICS CONTROL

K Number: K925256 · Decision Mar 1, 1993
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
38
Review Days
133

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Basic Information

Device Name
QUANTIMETRIX URINALYSIS MICROSCOPICS CONTROL
K Number
K925256
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Quantimetrix Corp.
Date Received
October 19, 1992
Decision Date
March 1, 1993
Product Code
JJY
Advisory Committee
Clinical Chemistry
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
JJY Multi-Analyte Controls, All Kinds (Assayed)

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K Number Device Name
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K103744 DROPPER A1C DIABETES CONTROL
K062942 QUANTIMETRIX NICOSURE COTININE URINE CONTROL
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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