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

LIQUISPX HDL/LDL LIQUID CHOLESTEROL CALIBRATOR

K Number: K010030 · Decision Feb 14, 2001
Classifications
1
FEI Numbers
107
Registration Numbers
107
Same Product Code
301
Applicant Total
1
Review Days
42

Basic Information

Device Name
LIQUISPX HDL/LDL LIQUID CHOLESTEROL CALIBRATOR
K Number
K010030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SYNERGENT BIOCHEM INC.-CLINICAL CONTROLS DIV.
Date Received
January 3, 2001
Decision Date
February 14, 2001
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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