G-Vitri Vitrification Freeze Media; G-Vitri Vitrification Thawing Media
K-Number: K232942 · 2024-01-30
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.