InVision™ 3T 充電式手術室
K 號：K252239 · 2025-08-06
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器材摘要
InVision™ 3T Recharge Operating Suite is the device name listed in this FDA 510(k) record. The listed applicant is Imris Imaging, Inc.. It received FDA 510(k) clearance on 2025-08-06 under 510(k) number K252239. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the InVision™ 3T Recharge Operating Suite?
InVision™ 3T Recharge Operating Suite is a medical device that received FDA 510(k) clearance on 2025-08-06. The listed applicant is Imris Imaging, Inc.. The 510(k) number is K252239.
When did InVision™ 3T Recharge Operating Suite receive FDA 510(k) clearance?
InVision™ 3T Recharge Operating Suite received FDA 510(k) clearance on 2025-08-06, under 510(k) number K252239.
Who is the listed applicant for InVision™ 3T Recharge Operating Suite?
The FDA 510(k) record lists Imris Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InVision™ 3T Recharge Operating Suite?
The FDA product code for InVision™ 3T Recharge Operating Suite is LNH.
相關臨床試驗
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相關器械（代碼：LNH）
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。
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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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