FDA 510(k) Application Details - K053509

Device Classification Name	Device, Acupressure   More FDA Info for this Device
510(K) Number	K053509
Device Name	Device, Acupressure
Applicant	ACUBAND INC. 101 LITTLE SILVER POINT ROAD LITTLE SILVER, NJ 07739 US Other 510(k) Applications for this Company
Contact	RICHARD GRIFFITH 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	12/16/2005
Decision Date	08/16/2006
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