GE LOGIQ 700


the company

Device Classification Name

system, imaging, pulsed echo, ultrasonic

510(k) Number K000516
Device Name GE LOGIQ 700
Original Applicant
GE MEDICAL SYSTEMS, INC.
p.o. box 414
milwaukee, 
WI 
53201

Original Contact allen schuh
Regulation Number 892.1560
Classification Product Code
IYO  
Subsequent Product Codes
ITX   IYN  
Date Received 02/16/2000
Decision Date 04/19/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

Type Special
Reviewed by Third Party No

Combination Product

No