AIAS Cephalon
K号: K252214 · 2025-10-07
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器械摘要
AIAS Cephalon is the device name listed in this FDA 510(k) record. The listed applicant is Metamorphosis GmbH. It received FDA 510(k) clearance on 2025-10-07 under 510(k) number K252214. 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 AIAS Cephalon?
AIAS Cephalon is a medical device that received FDA 510(k) clearance on 2025-10-07. The listed applicant is Metamorphosis GmbH. The 510(k) number is K252214.
When did AIAS Cephalon receive FDA 510(k) clearance?
AIAS Cephalon received FDA 510(k) clearance on 2025-10-07, under 510(k) number K252214.
Who is the listed applicant for AIAS Cephalon?
The FDA 510(k) record lists Metamorphosis GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIAS Cephalon?
The FDA product code for AIAS Cephalon is QIH.
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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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