AIAS Cephalon
K 號：K252214 · 2025-10-07
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器材摘要
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.
常見問題
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.
相關臨床試驗
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相關器械（代碼：QIH）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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