Localite TMS導航器TS
K 號：K223577 · 2023-04-17
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器材摘要
Localite TMS Navigator TS is the device name listed in this FDA 510(k) record. The listed applicant is Localite GmbH. It received FDA 510(k) clearance on 2023-04-17 under 510(k) number K223577. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Localite TMS Navigator TS?
Localite TMS Navigator TS is a medical device that received FDA 510(k) clearance on 2023-04-17. The listed applicant is Localite GmbH. The 510(k) number is K223577.
When did Localite TMS Navigator TS receive FDA 510(k) clearance?
Localite TMS Navigator TS received FDA 510(k) clearance on 2023-04-17, under 510(k) number K223577.
Who is the listed applicant for Localite TMS Navigator TS?
The FDA 510(k) record lists Localite GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Localite TMS Navigator TS?
The FDA product code for Localite TMS Navigator TS is HAW.
相關臨床試驗
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相關器械（代碼：HAW）
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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