Scented Menstrual Pad
by Procter & Gamble Mfg. Co. 510(k)
Active
510(k) K842764
Overview
The Scented Menstrual Pad is a Class II medical device designed for feminine hygiene during menstruation. It is a pad with added scent or scented-deodorized properties, manufactured by Procter & Gamble Mfg. Co.
This device is supplied as a single-use product and is not indicated for MRI use. It is authorized under FDA 510(k) clearance with product code HHL and is regulated for use in obstetrics/gynecology settings. The device is stored at room temperature and has been cleared for marketing since 1984.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK842764 | Date10 Aug 1984 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- HHL
- Device Class
- Class II
- Regulation
- 21 CFR Part 884.5425
- Advisory Committee
- Obstetrics/Gynecology
- FDA Decision
- SESE Substantially Equivalent
Other devices from Procter & Gamble Co.
Questions
What is the Scented Menstrual Pad used for?
The Scented Menstrual Pad is a Class II medical device designed for feminine hygiene during menstruation. It features added scent or scented-deodorized properties to provide comfort and freshness during use.
Is the Scented Menstrual Pad reusable or single-use?
The Scented Menstrual Pad is supplied as a single-use product only. It should not be reused as this could compromise hygiene and effectiveness, and it is not indicated for MRI use.
How should the Scented Menstrual Pad be stored?
The Scented Menstrual Pad should be stored at room temperature. Proper storage conditions help maintain the integrity of the product's scent and absorbent properties until use.
What is the regulatory status of the Scented Menstrual Pad?
The Scented Menstrual Pad is authorized under FDA 510(k) clearance with product code HHL. It has been cleared for marketing since 1984 and is regulated for use in obstetrics/gynecology settings.