# K993870: Unscented Interlabial Menstrual Pad

- Pathway: 510(k) (Traditional)
- Applicant: Procter & Gamble Co.
- Decided: Jan 18, 2000 after 64 days
- Product code: HHD (Pad, Menstrual, Unscented)
- Device class: 1
- Regulation: 21 CFR 884.5435
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K844601 (1985). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K881384: Interlabial Pad, Xtramedics, Inc. (1989) Summary page 1.
- K844601: Unscented Menstrual Pad, Procter & Gamble Mfg. Co. (1985) Summary page 1.

## Indications for use
The Unscented Interiablal Menstrual Pad can be wom any time of the day or night in the following ways: Alone far light and medium (menstrual) flow In combination with tampons or Pads for extra protection during heavy (menstrual) flow Alone for vaginal discharge or slight urine loss associated with laughs, coughs, and sneezes.

Source page: https://510kreport.com/device/K993870
Methodology: https://510kreport.com/methodology