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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name spirometer, monitoring (w/wo alarm)
510(k) Number K890932
Device Name CAV 3.0C SOFTWARE PROGRAM
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 Number868.1850
Classification Product Code
BZK  
Date Received02/24/1989
Decision Date 06/12/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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