meddevicedb.com FDA Device Reference

CAREFREE(TM) FESTIVA PANTYSHIELDS

K901664 Class I Traditional
Decision Date
1990-06-22
Sponsor / Applicant
Personal Products Co.

Technical Specification

510(k) Submission ID K901664
Product Code HHD
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5435
Decision Date 1990-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAREFREE(TM) FESTIVA PANTYSHIELDS received FDA 510(k) clearance under submission number K901664, sponsored by Personal Products 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 1990-06-22.

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.