meddevicedb.com FDA Device Reference

Actively Trying Personal Lubricant Rose Scented

K212885 Class II Traditional
Decision Date
2022-02-11
Sponsor / Applicant
CC Wellness, LLC

Technical Specification

510(k) Submission ID K212885
Product Code PEB
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2022-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Actively Trying Personal Lubricant Rose Scented received FDA 510(k) clearance under submission number K212885, sponsored by CC Wellness, LLC. 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 2022-02-11.

Classification & Regulation

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