VIOGUARD SELF-SANITIZING KEYBOARD, MODEL UVKB50— 510(k) DEN100013

Unknown

Vioguard

FDA 510(k) clearance DEN100013 for VIOGUARD SELF-SANITIZING KEYBOARD, MODEL UVKB50, Unknown on 2011-12-20. Applicant: Vioguard. Device class: 2.

Clearance details

Applicant
Vioguard
Product code
Code OSZ
Device class
Class 2
Regulation
21 CFR 880.6600
Advisory panel
General Hospital
Date received
Decision date
Decision
Unknown
Clearance type
Post-NSE
Location
Bothell, WA, US
View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.