LOGIQ S7 EXPERT, LOGIQ S7 PRO


Device Classification Name

system, imaging, pulsed doppler, ultrasonic

510(k) Number K122114
Device Name LOGIQ S7 EXPERT, LOGIQ S7 PRO
Applicant
GE HEALTHCARE
9900 innovation drive
wauwatosa, 
WI 
53226

Applicant Contact bryan behn
Correspondent
GE HEALTHCARE
9900 innovation drive
wauwatosa, 
WI 
53226

Correspodent Contact bryan behn
Regulation Number 892.1550
Classification Product Code
IYN  
Subsequent Product Codes
ITX   IYO  
Date Received 07/17/2012
Decision Date 10/03/2012
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls