accufit
K 號：K223802 · 2023-10-06
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器材摘要
accufit is the device name listed in this FDA 510(k) record. The listed applicant is Mettler Electronics Corporation. It received FDA 510(k) clearance on 2023-10-06 under 510(k) number K223802. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the accufit?
accufit is a medical device that received FDA 510(k) clearance on 2023-10-06. The listed applicant is Mettler Electronics Corporation. The 510(k) number is K223802.
When did accufit receive FDA 510(k) clearance?
accufit received FDA 510(k) clearance on 2023-10-06, under 510(k) number K223802.
Who is the listed applicant for accufit?
The FDA 510(k) record lists Mettler Electronics Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for accufit?
The FDA product code for accufit is IPF.
相關臨床試驗
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。
其他以 Mettler Electronics Corporation 為申請人之記錄
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。
相關器械（代碼：IPF）
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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