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FDA 510(k) Application Details - K974009
Device Classification Name
Radioimmunoassay, Human Chorionic Gonadotropin
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510(K) Number
K974009
Device Name
Radioimmunoassay, Human Chorionic Gonadotropin
Applicant
INTERNATIONAL NEWTECH DEVELOPMENT, INC.
1629 FOSTERS WAY
DELTA, BRITISH COLUMBIA V3M 6S7 CA
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Contact
BENNY WANG
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Regulation Number
862.1155
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Classification Product Code
JHI
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More FDA Info for this Product Code
Date Received
10/21/1997
Decision Date
03/13/1998
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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