FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

PREVU POINT OF CARE SKIN STEROL TEST

K Number: K062092 · Decision Sep 15, 2006
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
79
Applicant Total
1
Review Days
53

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Basic Information

Device Name
PREVU POINT OF CARE SKIN STEROL TEST
K Number
K062092
Device Class
FDA class 1
Clearance Type
Special
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Unknown
Statement or Summary
Summary
Applicant
Premd, Inc.
Date Received
July 24, 2006
Decision Date
September 15, 2006
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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