CL24N
K 號：K222717 · 2022-10-31
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器材摘要
CL24N is the device name listed in this FDA 510(k) record. The listed applicant is Wide Corporation. It received FDA 510(k) clearance on 2022-10-31 under 510(k) number K222717. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CL24N?
CL24N is a medical device that received FDA 510(k) clearance on 2022-10-31. The listed applicant is Wide Corporation. The 510(k) number is K222717.
When did CL24N receive FDA 510(k) clearance?
CL24N received FDA 510(k) clearance on 2022-10-31, under 510(k) number K222717.
Who is the listed applicant for CL24N?
The FDA 510(k) record lists Wide Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CL24N?
The FDA product code for CL24N is PGY.
其他以 Wide Corporation 為申請人之記錄
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相關器械（代碼：PGY）
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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