Vitavitro 液氮冻存试剂盒,Vitavitro 加热试剂盒,以及 Vitavitro 管道套装
K号: K180073 · 2018-08-29
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器械摘要
常见问题
What is the Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set?
Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set is a medical device that received FDA 510(k) clearance on 2018-08-29. The listed applicant is Shenzhen Vitavitro Bio-Tech Co., Ltd.. The 510(k) number is K180073.
When did Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set receive FDA 510(k) clearance?
Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set received FDA 510(k) clearance on 2018-08-29, under 510(k) number K180073.
Who is the listed applicant for Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set?
The FDA 510(k) record lists Shenzhen Vitavitro Bio-Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set?
The FDA product code for Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set is MQL.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:MQL)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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