FDA 510(k) Application Details - K093322

Device Classification Name	Stimulator, Electro-Acupuncture   More FDA Info for this Device
510(K) Number	K093322
Device Name	Stimulator, Electro-Acupuncture
Applicant	UPC MEDICAL SUPPLIES, INC. DBA UNITED PACIFIC CO. 317 S. SAN MARINO AVE. SAN GABRIEL, CA 91776 US Other 510(k) Applications for this Company
Contact	DANIEL HUE Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	BWK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/23/2009
Decision Date	08/05/2010
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