meddevicedb.com FDA Device Reference

TAMPAX M PLASTIC TAMPONS, UNSCENTED

K133244 Class II Special
Decision Date
2014-01-09
Sponsor / Applicant
The Procter & Gamble Company

Technical Specification

510(k) Submission ID K133244
Product Code HEB
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5470
Decision Date 2014-01-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAMPAX M PLASTIC TAMPONS, UNSCENTED received FDA 510(k) clearance under submission number K133244, sponsored by The Procter & Gamble Company. The device was reviewed via the Special premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2014-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code HEB and 21 CFR 884.5470, within the Obstetrics/Gynecology review panel as a Class II device.