FDA 510(k) Application Details - K110821

Device Classification Name	Device, Acupressure   More FDA Info for this Device
510(K) Number	K110821
Device Name	Device, Acupressure
Applicant	DOODLEBUG PRODUCTS, LLC 5 HEMINGWAY LANE WEST NEWBURY, MA 01985 US Other 510(k) Applications for this Company
Contact	BARRY E SANDS 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	03/24/2011
Decision Date	02/27/2012
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