MODIFIED REGULAR MAXITHINS PADS, UNSCENTED

Pad, Menstrual, Unscented

TAMBRANDS, INC.

The following data is part of a premarket notification filed by Tambrands, Inc. with the FDA for Modified Regular Maxithins Pads, Unscented.

Pre-market Notification Details

Device IDK862680
510k NumberK862680
Device Name:MODIFIED REGULAR MAXITHINS PADS, UNSCENTED
ClassificationPad, Menstrual, Unscented
Applicant TAMBRANDS, INC. BRIDGE & SPRINGFIELD STREETS Palmer,  MA  01069
ContactStaab, Phd
CorrespondentStaab, Phd
TAMBRANDS, INC. BRIDGE & SPRINGFIELD STREETS Palmer,  MA  01069
Product CodeHHD  
CFR Regulation Number884.5435 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-07-14
Decision Date1986-08-15

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