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K 號：K241495 · 2024-11-21
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器材摘要
Jazz Classic is the device name listed in this FDA 510(k) record. The listed applicant is Jazz Imaging. It received FDA 510(k) clearance on 2024-11-21 under 510(k) number K241495. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Jazz Classic?
Jazz Classic is a medical device that received FDA 510(k) clearance on 2024-11-21. The listed applicant is Jazz Imaging. The 510(k) number is K241495.
When did Jazz Classic receive FDA 510(k) clearance?
Jazz Classic received FDA 510(k) clearance on 2024-11-21, under 510(k) number K241495.
Who is the listed applicant for Jazz Classic?
The FDA 510(k) record lists Jazz Imaging as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Jazz Classic?
The FDA product code for Jazz Classic is LLZ.
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相關器械（代碼：LLZ）
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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