PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02


Device Classification Name

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

510(k) Number K021422
Device Name PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02
Original Applicant
PHILIPS MEDICAL SYSTEMS
3000 minuteman rd.
andover, 
MA 
01810

Original Contact dave osborn
Regulation Number 870.1025
Classification Product Code
MHX  
Date Received 05/03/2002
Decision Date 05/15/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No