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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, Scented, Scented-Deodorized
510(k) Number K884429
Device Name ALWAYS SCENTED OR SCENTED DEODORIZED MENSTRUAL PAD
Applicant
Procter & Gamble Co.
Legal Division
1 Procter & Gamble Plz.
Cincinnati,  OH  45202
Applicant Contact T O'REILLY
Correspondent
Procter & Gamble Co.
Legal Division
1 Procter & Gamble Plz.
Cincinnati,  OH  45202
Correspondent Contact T O'REILLY
Regulation Number884.5425
Classification Product Code
HHL  
Date Received10/20/1988
Decision Date 12/02/1988
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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