Atlas FDA

VIOGUARD SELF-SANITIZING KEYBOARD, MODEL UVKB50

FDA 510(k) clearance DEN100013 · decided 2011-12-20

Clearance details

K-number
DEN100013
Device name
VIOGUARD SELF-SANITIZING KEYBOARD, MODEL UVKB50
Applicant
Vioguard
Decision
Unknown
Date received
2010-11-05
Decision date
2011-12-20
Days to decision
410 days
Clearance type
Post-NSE
Product code
OSZ
Device class
2
Regulation number
880.6600
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Bothell, WA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.