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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name valve, non-rebreathing
510(k) Number K781920
Device Name VALVE, VENT-AWAY TWO-WAY
Applicant
CHESEBROUGH-POND'S U.S.A. CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
CHESEBROUGH-POND'S U.S.A. CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5870
Classification Product Code
CBP  
Date Received11/13/1978
Decision Date 12/04/1978
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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