FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

VIOGUARD SELF-SANITIZING KEYBOARD, MODEL UVKB50

K Number: DEN100013 · Decision Dec 20, 2011
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
0
Applicant Total
1
Review Days
410

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VIOGUARD SELF-SANITIZING KEYBOARD, MODEL UVKB50
K Number
DEN100013
Device Class
FDA class 2
Clearance Type
Post-NSE
Regulation Number
880.6600
Medical Specialty
General Hospital
Decision
Unknown
Applicant
Vioguard
Date Received
November 5, 2010
Decision Date
December 20, 2011
Product Code
OSZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OSZ Antimicrobial Keyboard