FDA 510(k) Application Details - DEN100013

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN100013
Device Name	VIOGUARD SELF-SANITIZING KEYBOARD, MODEL UVKB50
Applicant	VIOGUARD 1725 220TH ST SE SUITE 201 BOTHELL, WA 98021 US Other 510(k) Applications for this Company
Contact	CRAIG RANTA Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OSZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/05/2010
Decision Date	12/20/2011
Decision	DENG -
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review