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FDA 510(k)

G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media

K-Number: K232942 · 2024-01-30

Decision Date2024-01-30
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media is a medical device manufactured by Gimbo Medical Technology Shenzhen Co., Ltd.. It received FDA 510(k) clearance on 2024-01-30 under approval number K232942. 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 G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media?

G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media is a medical device that received FDA 510(k) clearance on 2024-01-30. It is manufactured by Gimbo Medical Technology Shenzhen Co., Ltd.. The 510(k) number is K232942.

When was G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media approved by the FDA?

G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media received FDA 510(k) clearance on 2024-01-30, under approval number K232942.

What company makes G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media?

G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media is manufactured by Gimbo Medical Technology Shenzhen Co., Ltd..

What is the FDA product code for G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media?

The FDA product code for G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media is MQL.

Other Devices by Gimbo Medical Technology Shenzhen Co., Ltd.

Related Devices (Code: MQL)

Official Source

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