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FDA 510(k)

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

K-Number: K254261 · 2026-08-28

Decision Date2026-08-28
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK) is the device name listed in this FDA 510(k) record. The listed applicant is CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.. It received FDA 510(k) clearance on 2026-08-28 under 510(k) number K254261. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)?

Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK) is a medical device that received FDA 510(k) clearance on 2026-08-28. The listed applicant is CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.. The 510(k) number is K254261.

When did Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK) receive FDA 510(k) clearance?

Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK) received FDA 510(k) clearance on 2026-08-28, under 510(k) number K254261.

Who is the listed applicant for Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)?

The FDA 510(k) record lists CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)?

The FDA product code for Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK) is MQL.

Related Devices (Code: MQL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.