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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name system, abortion, vacuum
510(k) Number K880734
Device Name SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS
Applicant
PERSONAL PRODUCTS CO.
MILLTOWN,  NJ  08850
Applicant Contact A. J HUETTEMAN
Correspondent
PERSONAL PRODUCTS CO.
MILLTOWN,  NJ  08850
Correspondent Contact A. J HUETTEMAN
Regulation Number884.5070
Classification Product Code
HHI  
Date Received02/24/1988
Decision Date 04/25/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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