Gynatrof
K号: K232040 · 2024-03-01
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决定日期2024-03-01
产品代码NUC
咨询委员会OB
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器械摘要
Gynatrof is the device name listed in this FDA 510(k) record. The listed applicant is Tyros Biopharma, Inc.. It received FDA 510(k) clearance on 2024-03-01 under 510(k) number K232040. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Gynatrof?
Gynatrof is a medical device that received FDA 510(k) clearance on 2024-03-01. The listed applicant is Tyros Biopharma, Inc.. The 510(k) number is K232040.
When did Gynatrof receive FDA 510(k) clearance?
Gynatrof received FDA 510(k) clearance on 2024-03-01, under 510(k) number K232040.
Who is the listed applicant for Gynatrof?
The FDA 510(k) record lists Tyros Biopharma, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Gynatrof?
The FDA product code for Gynatrof is NUC.
相关临床试验
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相关器械（代码：NUC）
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。
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官方来源
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