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FDA 510(k) Application Details - K010244
Device Classification Name
Radioimmunoassay, Luteinizing Hormone
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510(K) Number
K010244
Device Name
Radioimmunoassay, Luteinizing Hormone
Applicant
Chembio Diagnostic Systems, Inc.
163 CABOT ST.
BEVERLY,, MA 01915 US
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Contact
FRAN WHITE
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Regulation Number
862.1485
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Classification Product Code
CEP
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More FDA Info for this Product Code
Date Received
01/25/2001
Decision Date
05/02/2001
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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