meddevicedb.com FDA Device Reference

Replens Long-Lasting Vaginal Moisturizer

K203818 Class II Traditional
Decision Date
2021-06-11
Sponsor / Applicant
Church & Dwight Co., Inc.

Technical Specification

510(k) Submission ID K203818
Product Code NUC
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2021-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Replens Long-Lasting Vaginal Moisturizer received FDA 510(k) clearance under submission number K203818, sponsored by Church & Dwight Co., 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 2021-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code NUC and 21 CFR 884.5300, within the Obstetrics/Gynecology review panel as a Class II device.