meddevicedb.com FDA Device Reference

UNSCENTED MENSTRUAL PADS

K812577 Class I Traditional
Decision Date
1981-10-19
Sponsor / Applicant
Weyerhaeuser Co.

Technical Specification

510(k) Submission ID K812577
Product Code HHD
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5435
Decision Date 1981-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNSCENTED MENSTRUAL PADS received FDA 510(k) clearance under submission number K812577, sponsored by Weyerhaeuser Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1981-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code HHD and 21 CFR 884.5435, within the Obstetrics/Gynecology review panel as a Class I device.