Exablate 模型 2100V1,Exablate 前列腺系統,Exablate MRgFUS,Exablate 2100V1 型號 3.0
K 號:K231378 · 2023-10-30
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器材摘要
常見問題
What is the Exablate Model 2100V1, Exablate Prostate System, Exablate MRgFUS, Exablate 2100V1 Type 3.0?
Exablate Model 2100V1, Exablate Prostate System, Exablate MRgFUS, Exablate 2100V1 Type 3.0 is a medical device that received FDA 510(k) clearance on 2023-10-30. The listed applicant is Insightec, Ltd.. The 510(k) number is K231378.
When did Exablate Model 2100V1, Exablate Prostate System, Exablate MRgFUS, Exablate 2100V1 Type 3.0 receive FDA 510(k) clearance?
Exablate Model 2100V1, Exablate Prostate System, Exablate MRgFUS, Exablate 2100V1 Type 3.0 received FDA 510(k) clearance on 2023-10-30, under 510(k) number K231378.
Who is the listed applicant for Exablate Model 2100V1, Exablate Prostate System, Exablate MRgFUS, Exablate 2100V1 Type 3.0?
The FDA 510(k) record lists Insightec, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Exablate Model 2100V1, Exablate Prostate System, Exablate MRgFUS, Exablate 2100V1 Type 3.0?
The FDA product code for Exablate Model 2100V1, Exablate Prostate System, Exablate MRgFUS, Exablate 2100V1 Type 3.0 is PLP.
相關臨床試驗
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相關器械(代碼:PLP)
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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