Ablation-fit
K 號：K222938 · 2023-09-12
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器材摘要
Ablation-fit is the device name listed in this FDA 510(k) record. The listed applicant is R.A.W. S.R.L. It received FDA 510(k) clearance on 2023-09-12 under 510(k) number K222938. The device is classified under product code QTZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Ablation-fit?
Ablation-fit is a medical device that received FDA 510(k) clearance on 2023-09-12. The listed applicant is R.A.W. S.R.L. The 510(k) number is K222938.
When did Ablation-fit receive FDA 510(k) clearance?
Ablation-fit received FDA 510(k) clearance on 2023-09-12, under 510(k) number K222938.
Who is the listed applicant for Ablation-fit?
The FDA 510(k) record lists R.A.W. S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ablation-fit?
The FDA product code for Ablation-fit is QTZ.
相關臨床試驗
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相關器械（代碼：QTZ）
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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