meddevicedb.com FDA Device Reference

PRIVATE LABEL DEODORANT MAXISHIELD

K831691 Class II Traditional
Decision Date
1983-06-30
Sponsor / Applicant
Int'L Consumer Disposables

Technical Specification

510(k) Submission ID K831691
Product Code HHL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5425
Decision Date 1983-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRIVATE LABEL DEODORANT MAXISHIELD received FDA 510(k) clearance under submission number K831691, sponsored by Int'L Consumer Disposables. 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 1983-06-30.

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.