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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name saliva, artificial
510(k) Number K091419
Device Name VICKS POWERSHOT DRY THROAT & MOUTH RELIEF
Applicant
THE PROCTER & GAMBLE CO.
8700 MASON-MONTGOMERY ROAD
MASON,  OH  45040
Applicant Contact RICHARD J COOKE
Correspondent
THE PROCTER & GAMBLE CO.
8700 MASON-MONTGOMERY ROAD
MASON,  OH  45040
Correspondent Contact RICHARD J COOKE
Classification Product Code
LFD  
Date Received05/13/2009
Decision Date 08/28/2009
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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