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

CHOLESTRAK HDL CHOLESTEROL HOME TEST

K Number: K072836 · Decision Dec 27, 2007
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
79
Applicant Total
1
Review Days
85

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Basic Information

Device Name
CHOLESTRAK HDL CHOLESTEROL HOME TEST
K Number
K072836
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Accutech, LLC
Date Received
October 3, 2007
Decision Date
December 27, 2007
Product Code
LBS
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
LBS Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl

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