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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Ventilator, Continuous, Facility Use
510(k) Number K890921
Device Name DATA EXCHANGE SYSTEM, MODEL 24
Applicant
Siemens Life Support Systems
P.O. Box 68517
Schaumberg,  IL  60168
Applicant Contact ELLEN FARNEY
Correspondent
Siemens Life Support Systems
P.O. Box 68517
Schaumberg,  IL  60168
Correspondent Contact ELLEN FARNEY
Regulation Number868.5895
Classification Product Code
CBK  
Date Received02/24/1989
Decision Date 06/08/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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