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FDA 510(k) Application Details - K020567
Device Classification Name
Device, Galvanic Skin Response Measurement
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510(K) Number
K020567
Device Name
Device, Galvanic Skin Response Measurement
Applicant
VIBRANT HEALTH
150 DES GRANDS COTEAUX
BEOEIL, QUEBEC J3G 2C9 CA
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Contact
STEPHEN EMOND
Other 510(k) Applications for this Contact
Regulation Number
882.1540
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Classification Product Code
GZO
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More FDA Info for this Product Code
Date Received
02/20/2002
Decision Date
05/02/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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