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FDA 510(k) Application Details - K002874
Device Classification Name
Stimulator, Nerve, Transcutaneous, For Pain Relief
More FDA Info for this Device
510(K) Number
K002874
Device Name
Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant
WELL-LIFE CONSULTANT
6CO1,NO.5.SEC.5,HSIN YI RD.
TAIPEI TW
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Contact
KEVIN CHIU
Other 510(k) Applications for this Contact
Regulation Number
882.5890
More FDA Info for this Regulation Number
Classification Product Code
GZJ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/14/2000
Decision Date
07/27/2001
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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