夜巡+ US
K 號：K243199 · 2025-07-12
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器材摘要
NightWatch+ US is the device name listed in this FDA 510(k) record. The listed applicant is Livassured BV. It received FDA 510(k) clearance on 2025-07-12 under 510(k) number K243199. The device is classified under product code POS. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NightWatch+ US?
NightWatch+ US is a medical device that received FDA 510(k) clearance on 2025-07-12. The listed applicant is Livassured BV. The 510(k) number is K243199.
When did NightWatch+ US receive FDA 510(k) clearance?
NightWatch+ US received FDA 510(k) clearance on 2025-07-12, under 510(k) number K243199.
Who is the listed applicant for NightWatch+ US?
The FDA 510(k) record lists Livassured BV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NightWatch+ US?
The FDA product code for NightWatch+ US is POS.
相關臨床試驗
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相關器械（代碼：POS）
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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