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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 K926161
Device Name RES Q AIR SYSTEM MODEL HT-1000
Applicant
C.F. ELECTRONICS, INC.
56 WESTCOTT RD.
STAMFORD,  CT  06902
Applicant Contact CORNELIA DAMSKY
Correspondent
C.F. ELECTRONICS, INC.
56 WESTCOTT RD.
STAMFORD,  CT  06902
Correspondent Contact CORNELIA DAMSKY
Regulation Number868.5450
Classification Product Code
BTT  
Date Received12/08/1992
Decision Date 08/26/1993
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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