FDA 510(k) Application Details - K142471

Device Classification Name	Device, Acupressure   More FDA Info for this Device
510(K) Number	K142471
Device Name	Device, Acupressure
Applicant	Pressure Point Inc. 936 Green Meadow Drive Tinton Falls, NJ 07724 US Other 510(k) Applications for this Company
Contact	Joseph DiLustro Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MVV Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/03/2014
Decision Date	12/01/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review