KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392E


Device Classification Name

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

510(k) Number K010923
Device Name KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392E
Original Applicant
SIEMENS ELEMA AB
medical solutions
186 wood avenue south
iselin, 
NJ 
08830 -2770

Original Contact diane wurzburger
Regulation Number 870.1025
Classification Product Code
MHX  
Subsequent Product Code
BSZ  
Date Received 03/27/2001
Decision Date 01/23/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

Type Abbreviated
Reviewed by Third Party No

Combination Product

No

Category: Uncategorized