JLK-CTP
K 號：K242556 · 2024-10-16
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器材摘要
JLK-CTP is the device name listed in this FDA 510(k) record. The listed applicant is JLK, Inc.. It received FDA 510(k) clearance on 2024-10-16 under 510(k) number K242556. 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 JLK-CTP?
JLK-CTP is a medical device that received FDA 510(k) clearance on 2024-10-16. The listed applicant is JLK, Inc.. The 510(k) number is K242556.
When did JLK-CTP receive FDA 510(k) clearance?
JLK-CTP received FDA 510(k) clearance on 2024-10-16, under 510(k) number K242556.
Who is the listed applicant for JLK-CTP?
The FDA 510(k) record lists JLK, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JLK-CTP?
The FDA product code for JLK-CTP is LLZ.
其他以 JLK, Inc. 為申請人之記錄
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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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