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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pad, Menstrual, Unscented
510(k) Number K850955
Device Name ALWAYS MAXIPADS - UNSCENTED
Applicant
Procter & Gamble Mfg. Co.
P.O. Box 599
Cincinnati,  OH  45201
Applicant Contact JAMES T O'REILLY
Correspondent
Procter & Gamble Mfg. Co.
P.O. Box 599
Cincinnati,  OH  45201
Correspondent Contact JAMES T O'REILLY
Regulation Number884.5435
Classification Product Code
HHD  
Date Received03/08/1985
Decision Date 05/14/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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