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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
510(k) Number K840279
Device Name DRAGER BAROMED
Applicant
DRAEGER MEDICAL, INC.
PA 
Correspondent
DRAEGER MEDICAL, INC.
PA 
Regulation Number868.2600
Classification Product Code
CAP  
Date Received01/23/1984
Decision Date 03/02/1984
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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