MODIFICATION TO: MUSE CARDIOLOGY INFORMATION SYSTEM


Device Classification Name

computer, diagnostic, programmable

510(k) Number K072502
Device Name MODIFICATION TO: MUSE CARDIOLOGY INFORMATION SYSTEM
Applicant
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
9900 innavation dr.
wauwatosa, 
WI 
53226

Applicant Contact patricia taige
Correspondent
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
9900 innavation dr.
wauwatosa, 
WI 
53226

Correspodent Contact patricia taige
Regulation Number 870.1425
Classification Product Code
DQK  
Date Received 09/06/2007
Decision Date 11/19/2007
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls