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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
510(k) Number K905296
Device Name CHOLESTECH LIPID MONITORING SYSTEM,HDL CHOLESTEROL
Applicant
Cholestech Corp.
3347 Investment Blvd.
Hayward,  CA  94545
Applicant Contact SUSAN WILLSON
Correspondent
Cholestech Corp.
3347 Investment Blvd.
Hayward,  CA  94545
Correspondent Contact SUSAN WILLSON
Regulation Number862.1475
Classification Product Code
LBS  
Date Received11/27/1990
Decision Date 12/26/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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