Unscented Interlabial Menstrual Pad

FDA 510(k) K993870 · Procter & Gamble Co.

Substantially Equivalent

510(k) numberK993870

Submission

Device name
Unscented Interlabial Menstrual Pad
Applicant
Procter & Gamble Co.
Cincinnati, OH, US
Received
November 15, 1999
Decision date
January 18, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HHD – Pad, Menstrual, Unscented
Device class
Class I (low risk)
Regulation
21 CFR 884.5435
Specialty
Obstetrics/Gynecology

An unscented menstrual pad which is used to absorb menstrual fluid or other vaginal discharge and is made of common cellulosic and synthetic material with an established safety profile.

Other 510(k)s with product code HHD

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K071827Always Menstrual PadsHHD · Traditional Procter & Gamble, Inc.09/20/2007SE
K012629Always DuetsHHD · Traditional Procter & Gamble Co.10/05/2001SE
K003843Envive MiniformsHHD · Traditional Procter & Gamble Co.02/08/2001SE
K980395Gladrags Cotton Menstrual PadHHD · Traditional Keepers!, Inc.04/16/1998SE
K953470Flushies Flushable/Biodegradable Menstrual Pads/Napkins (Ultra Thins)HHD · Traditional Mediquip, Inc.11/21/1995SE
K953668Unscented Ultrathin Maxi PadHHD · Traditional Paragon Trade Brands, Inc.11/01/1995SE
K953667Unscented Curved Ultrathin Maxi PadsHHD · Traditional Paragon Trade Brands, Inc.11/01/1995SE
K953633Unscented Menstrual PadHHD · Traditional Tendasoft, Inc.11/01/1995SE
K953553Unscented Menstral PadHHD · Traditional Paragon Trade Brands, Inc.10/27/1995SE
K953517Unscented Menstrual PadHHD · Traditional Paragon Trade Brands, Inc.10/26/1995SE

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K113699Tampax(R) V Plastic Applicator Tampons, UnscentedHEB · Special 01/12/2012SE
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Questions and answers

When was Unscented Interlabial Menstrual Pad cleared by the FDA?

Unscented Interlabial Menstrual Pad (K993870) received a 510(k) decision of Substantially Equivalent on January 18, 2000, 64 days after the submission was received.

What is the product code of K993870?

The FDA product code is HHD – Pad, Menstrual, Unscented, a Class I (low risk) device regulated under 21 CFR 884.5435.