GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM


Device Classification Name

system, imaging, pulsed echo, ultrasonic

510(k) Number K992208
Device Name GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM
Applicant
GE MEDICAL SYSTEMS, INC.
p.o. box 414
milwaukee, 
WI 
53201

Applicant Contact allen schuh
Regulation Number 892.1560
Classification Product Code
IYO  
Subsequent Product Code
ITX  
Date Received 06/30/1999
Decision Date 07/12/1999
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Traditional
Reviewed by Third Party Yes

Combination Product

No