LITE WAND II


Device Classification Name

light, surgical, fiberoptic

510(k) Number K080962
Device Name LITE WAND II
Applicant
THOMPSON SURGICAL INSTRUMENTS, INC.
10170 east cherry bend road
traverse city, 
MI 
49684

Applicant Contact stephanie a zalucha
Correspondent
THOMPSON SURGICAL INSTRUMENTS, INC.
10170 east cherry bend road
traverse city, 
MI 
49684

Correspodent Contact stephanie a zalucha
Regulation Number 878.4580
Classification Product Code
FST  
Date Received 04/04/2008
Decision Date 06/25/2008
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