VERSA LITE


Device Classification Name

light, ultraviolet, dermatological

510(k) Number K073503
Device Name VERSA LITE
Applicant
DIOMEDICS, INC.
24372 mccloud ct.
laguna niguel, 
CA 
92677

Applicant Contact gary mocnik
Correspondent
DIOMEDICS, INC.
24372 mccloud ct.
laguna niguel, 
CA 
92677

Correspodent Contact gary mocnik
Regulation Number 878.4630
Classification Product Code
FTC  
Date Received 12/13/2007
Decision Date 01/23/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

Type Traditional
Reviewed by Third Party No

Combination Product

No