meddevicedb.com FDA Device Reference

Wet Organics Personal Lubricant

K182027 Class II Traditional
Decision Date
2018-11-21
Sponsor / Applicant
Trigg Laboratories Dba Wet International

Technical Specification

510(k) Submission ID K182027
Product Code NUC
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2018-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Wet Organics Personal Lubricant received FDA 510(k) clearance under submission number K182027, sponsored by Trigg Laboratories Dba Wet International. 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 2018-11-21.

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.