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FDA 510(k) Application Details - K982341
Device Classification Name
Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
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510(K) Number
K982341
Device Name
Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
Applicant
RANDOX LABORATORIES, LTD.
ARDMORE, DIAMOND ROAD
CRUMLIN, CO. ANTRIM BT29 4QY GB
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P ARMSTRONG
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Regulation Number
862.1475
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Classification Product Code
LBS
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Date Received
06/22/1998
Decision Date
07/30/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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