meddevicedb.com FDA Device Reference

Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)

K254261 Class II Traditional
Decision Date
2026-08-28
Sponsor / Applicant
CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.

Technical Specification

510(k) Submission ID K254261
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2026-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK) received FDA 510(k) clearance under submission number K254261, sponsored by CELL STORE (BEIJING) BIOTECHNOLOGY CO., 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 2026-08-28.

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.