SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS


Device Classification Name

monitor, physiological, patient(with arrhythmia detection or alarms)

510(k) Number K023569
Device Name SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS
Original Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
16 electronics ave.
danvers, 
MA 
01923

Original Contact penelope h greco
Regulation Number 870.1025
Classification Product Code
MHX  
Date Received 10/24/2002
Decision Date 11/04/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No