FDA 510(k) Application Details - K171802

Device Classification Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter   More FDA Info for this Device
510(K) Number	K171802
Device Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter
Applicant	Bayer HealthCare LLC 100 Bayer Boulevard Whippany, NJ 07981-0915 US Other 510(k) Applications for this Company
Contact	Cindy R. Abraham 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	06/19/2017
Decision Date	03/07/2018
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