ULTRAGUIDE CTG 2000SA


Device Classification Name

system, x-ray, tomography, computed

510(k) Number K022354
Device Name ULTRAGUIDE CTG 2000SA
Original Applicant
ULTRAGUIDE LTD.
377 route 17 south
hasbrouck heights, 
NJ 
07601

Original Contact george myers
Regulation Number 892.1750
Classification Product Code
JAK  
Date Received 07/19/2002
Decision Date 08/13/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No