MAGLIFE C/MAGLIFE C PLUS


Device Classification Name

monitor,physiological,patient(without arrhythmia detection or alarms)

510(k) Number K023195
Device Name MAGLIFE C/MAGLIFE C PLUS
Original Applicant
SCHILLER MEDICAL S.A.
4 rue louis pasteur
zae sud bp 90050
wissembourg cedex, 

FR

67162

Original Contact court goehry
Regulation Number 870.2300
Classification Product Code
MWI  
Date Received 09/25/2002
Decision Date 06/03/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No