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Gems Vitrification Set, Gems Warming Set

K162409 Class II Traditional
Decision Date
2017-05-24
Sponsor / Applicant
Genea Biomedx Pty, Ltd.

Technical Specification

510(k) Submission ID K162409
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2017-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Gems Vitrification Set, Gems Warming Set received FDA 510(k) clearance under submission number K162409, sponsored by Genea Biomedx Pty, Ltd.. 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 2017-05-24.

Classification & Regulation

This clearance is catalogued under FDA product code MQL and 21 CFR 884.6180, within the Obstetrics/Gynecology review panel as a Class II device.