meddevicedb.com FDA Device Reference

STAYFREE* DEODORANT MAXI-PADS

K834302 Class II Traditional
Decision Date
1984-01-17
Sponsor / Applicant
Johnson & Johnson Professionals, Inc.

Technical Specification

510(k) Submission ID K834302
Product Code HHL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5425
Decision Date 1984-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STAYFREE* DEODORANT MAXI-PADS received FDA 510(k) clearance under submission number K834302, sponsored by Johnson & Johnson Professionals, Inc.. 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 1984-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code HHL and 21 CFR 884.5425, within the Obstetrics/Gynecology review panel as a Class II device.