Neosoma 脑转移
K号: K252922 · 2025-12-17
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器械摘要
Neosoma Brain Mets is the device name listed in this FDA 510(k) record. The listed applicant is Neosoma, Inc.. It received FDA 510(k) clearance on 2025-12-17 under 510(k) number K252922. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Neosoma Brain Mets?
Neosoma Brain Mets is a medical device that received FDA 510(k) clearance on 2025-12-17. The listed applicant is Neosoma, Inc.. The 510(k) number is K252922.
When did Neosoma Brain Mets receive FDA 510(k) clearance?
Neosoma Brain Mets received FDA 510(k) clearance on 2025-12-17, under 510(k) number K252922.
Who is the listed applicant for Neosoma Brain Mets?
The FDA 510(k) record lists Neosoma, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Neosoma Brain Mets?
The FDA product code for Neosoma Brain Mets is QIH.
相关临床试验
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列明Neosoma, Inc.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：QIH）
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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