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FDA 510(k) Application Details - K072395
Device Classification Name
Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
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510(K) Number
K072395
Device Name
Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
Applicant
DIAZYME LABORATORIES
12889 GREGG COURT
POWAY, CA 92064 US
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Contact
CHARLES YU
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Regulation Number
862.1475
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Classification Product Code
LBS
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More FDA Info for this Product Code
Date Received
08/27/2007
Decision Date
01/03/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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