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WET PLATINUM PERSONAL LUBRICANT

K130012 Class II Traditional
Decision Date
2013-08-22
Sponsor / Applicant
Trigg Laboratories, Inc.

Technical Specification

510(k) Submission ID K130012
Product Code NUC
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2013-08-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WET PLATINUM PERSONAL LUBRICANT received FDA 510(k) clearance under submission number K130012, sponsored by Trigg Laboratories, 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 2013-08-22.

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.