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FDA 510(k) Application Details - K072799
Device Classification Name
Electrode, Cutaneous
More FDA Info for this Device
510(K) Number
K072799
Device Name
Electrode, Cutaneous
Applicant
VISION QUEST INDUSTRIES, INC.
18011 MITCHELL SO.
IRVINE, CA 92614 US
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Contact
JAIME X PULLEY
Other 510(k) Applications for this Contact
Regulation Number
882.1320
More FDA Info for this Regulation Number
Classification Product Code
GXY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/01/2007
Decision Date
04/24/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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