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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Humidifier, Respiratory Gas, (Direct Patient Interface)
510(k) Number K900854
Device Name JOHN BUNN: MEDIX COMPACT TRAVELLER
Applicant
The John Bunn Co.
290 Creekside Dr.
Tonawanda,  NY  14150
Applicant Contact RALPH L FULL
Correspondent
The John Bunn Co.
290 Creekside Dr.
Tonawanda,  NY  14150
Correspondent Contact RALPH L FULL
Regulation Number868.5450
Classification Product Code
BTT  
Date Received02/22/1990
Decision Date 04/23/1990
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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