MOBILE VERSA LIGHT


Device Classification Name

light, ultraviolet, dermatological

510(k) Number K111049
Device Name MOBILE VERSA LIGHT
Applicant
MEDTEK LIGHTING CORP
1131 anthem view lane
knoxville, 
TN 
37922

Applicant Contact robert wagner
Correspondent
MEDTEK LIGHTING CORP
1131 anthem view lane
knoxville, 
TN 
37922

Correspodent Contact robert wagner
Regulation Number 878.4630
Classification Product Code
FTC  
Date Received 04/15/2011
Decision Date 05/25/2012
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No