LIGHT GUIDE CABLE


Device Classification Name

illuminator, fiberoptic, surgical field

510(k) Number K111342
Device Name LIGHT GUIDE CABLE
Applicant
SCHOTT NORTH AMERICA
40 plain street
north attleboro, 
MA 
02760

Applicant Contact jeffrey roberts
Correspondent
SCHOTT NORTH AMERICA
40 plain street
north attleboro, 
MA 
02760

Correspodent Contact jeffrey roberts
Regulation Number 878.4580
Classification Product Code
HBI  
Date Received 05/13/2011
Decision Date 11/25/2011
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