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FDA 510(k) Application Details - K973102
Device Classification Name
Enzyme Immunoassay, Lidocaine
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510(K) Number
K973102
Device Name
Enzyme Immunoassay, Lidocaine
Applicant
DIAGNOSTIC REAGENTS, INC.
601 CALIFORNIA AVE.
SUNNYVALE, CA 94086 US
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Contact
YUH-GENG TSAY
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Regulation Number
862.3555
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Classification Product Code
KLR
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More FDA Info for this Product Code
Date Received
08/19/1997
Decision Date
09/12/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
TX - Clinical Toxicology
Review Advisory Committee
TX - Clinical Toxicology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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