FDA 510(k) Application Details - K041766

Device Classification Name	Device, Acupressure   More FDA Info for this Device
510(K) Number	K041766
Device Name	Device, Acupressure
Applicant	APOTHECARY PRODUCTS, INC. 11750 12TH AVE. SOUTH BURNSVILLE, MN 55337-1295 US Other 510(k) Applications for this Company
Contact	DAVID KRAMER 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	06/30/2004
Decision Date	11/26/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review