meddevicedb.com FDA Device Reference

INTERNAL HYDRATING GEL

K141718 Class II Traditional
Decision Date
2014-11-13
Sponsor / Applicant
Combe Incorporated

Technical Specification

510(k) Submission ID K141718
Product Code NUC
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2014-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTERNAL HYDRATING GEL received FDA 510(k) clearance under submission number K141718, sponsored by Combe Incorporated. 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 2014-11-13.

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.