Cryotop 玻璃化试剂盒和 Cryotop 解冻试剂盒
K号: K160864 · 2016-10-07
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器械摘要
常见问题
What is the Cryotop Vitrification Kit and Cryotop Thawing Kit?
Cryotop Vitrification Kit and Cryotop Thawing Kit is a medical device that received FDA 510(k) clearance on 2016-10-07. The listed applicant is Kitazato Biopharma Co., Ltd.. The 510(k) number is K160864.
When did Cryotop Vitrification Kit and Cryotop Thawing Kit receive FDA 510(k) clearance?
Cryotop Vitrification Kit and Cryotop Thawing Kit received FDA 510(k) clearance on 2016-10-07, under 510(k) number K160864.
Who is the listed applicant for Cryotop Vitrification Kit and Cryotop Thawing Kit?
The FDA 510(k) record lists Kitazato Biopharma Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cryotop Vitrification Kit and Cryotop Thawing Kit?
The FDA product code for Cryotop Vitrification Kit and Cryotop Thawing Kit is MQL.
相关临床试验
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列明Kitazato Biopharma Co., Ltd.为申报人的其他记录
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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