NET Recovery Corp/NET 製備 医療設備 監管文本
K 號：K233166 · 2024-05-29
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器材摘要
NET Recovery Corp/NET Device is the device name listed in this FDA 510(k) record. The listed applicant is Net Recovery. It received FDA 510(k) clearance on 2024-05-29 under 510(k) number K233166. The device is classified under product code PZR. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NET Recovery Corp/NET Device?
NET Recovery Corp/NET Device is a medical device that received FDA 510(k) clearance on 2024-05-29. The listed applicant is Net Recovery. The 510(k) number is K233166.
When did NET Recovery Corp/NET Device receive FDA 510(k) clearance?
NET Recovery Corp/NET Device received FDA 510(k) clearance on 2024-05-29, under 510(k) number K233166.
Who is the listed applicant for NET Recovery Corp/NET Device?
The FDA 510(k) record lists Net Recovery as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NET Recovery Corp/NET Device?
The FDA product code for NET Recovery Corp/NET Device is PZR.
相關臨床試驗
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。
相關器械（代碼：PZR）
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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