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FDA 510(k) Application Details - K131975
Device Classification Name
Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase
More FDA Info for this Device
510(K) Number
K131975
Device Name
Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase
Applicant
ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC.
4 HENDERSON DRIVE
WEST CALDWELL, NJ 07006 US
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Contact
HYMAN KATZ
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Regulation Number
862.1440
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Classification Product Code
CFJ
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More FDA Info for this Product Code
Date Received
06/28/2013
Decision Date
10/02/2013
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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