FDA 510(k) Application Details - K152374

Device Classification Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter   More FDA Info for this Device
510(K) Number	K152374
Device Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter
Applicant	Fuji Dynamics Ltd 1-3, 23/F., Laws Commercial Plaza, 788 Cheung Sha Wan Road Hong Kong CN Other 510(k) Applications for this Company
Contact	Man Man Chung Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	NUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/21/2015
Decision Date	01/13/2016
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