FDA 510(k) Application Details - DEN100024

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN100024
Device Name	ZAP-IT!
Applicant	ECOBRANDS LTD. 5401 S. COTTONWOOD CT. GREENWOOD VILLAGE, CO 80121 US Other 510(k) Applications for this Company
Contact	Kevin Walls Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OSG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/09/2010
Decision Date	11/07/2014
Decision	DENG -
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review