Idys® LIF
K 號：K243670 · 2024-12-31
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器材摘要
Idys® LIF is the device name listed in this FDA 510(k) record. The listed applicant is Clariance. It received FDA 510(k) clearance on 2024-12-31 under 510(k) number K243670. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Idys® LIF?
Idys® LIF is a medical device that received FDA 510(k) clearance on 2024-12-31. The listed applicant is Clariance. The 510(k) number is K243670.
When did Idys® LIF receive FDA 510(k) clearance?
Idys® LIF received FDA 510(k) clearance on 2024-12-31, under 510(k) number K243670.
Who is the listed applicant for Idys® LIF?
The FDA 510(k) record lists Clariance as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Idys® LIF?
The FDA product code for Idys® LIF is MAX.
其他以 Clariance 為申請人之記錄
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相關器械（代碼：MAX）
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。
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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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