ALWAYS SUPER MAXIPAD-UNSCENTED

Pad, Menstrual, Unscented

PROCTER & GAMBLE MFG. CO.

The following data is part of a premarket notification filed by Procter & Gamble Mfg. Co. with the FDA for Always Super Maxipad-unscented.

Pre-market Notification Details

Device IDK850940
510k NumberK850940
Device Name:ALWAYS SUPER MAXIPAD-UNSCENTED
ClassificationPad, Menstrual, Unscented
Applicant PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati,  OH  45201
ContactJames T O'reilly
CorrespondentJames T O'reilly
PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati,  OH  45201
Product CodeHHD  
CFR Regulation Number884.5435 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-03-07
Decision Date1985-05-14

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