meddevicedb.com FDA Device Reference

Sensual Massage, Ultra Pure

K211967 Class II Traditional
Decision Date
2021-11-09
Sponsor / Applicant
Dreambrands, Inc.

Technical Specification

510(k) Submission ID K211967
Product Code NUC
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2021-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sensual Massage, Ultra Pure received FDA 510(k) clearance under submission number K211967, sponsored by Dreambrands, 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 2021-11-09.

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.