AQUABEAM Robotic System (AB2000)
K 號：K241952 · 2024-09-30
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器材摘要
AQUABEAM Robotic System (AB2000) is the device name listed in this FDA 510(k) record. The listed applicant is Procept Biorobotics. It received FDA 510(k) clearance on 2024-09-30 under 510(k) number K241952. The device is classified under product code PZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the AQUABEAM Robotic System (AB2000)?
AQUABEAM Robotic System (AB2000) is a medical device that received FDA 510(k) clearance on 2024-09-30. The listed applicant is Procept Biorobotics. The 510(k) number is K241952.
When did AQUABEAM Robotic System (AB2000) receive FDA 510(k) clearance?
AQUABEAM Robotic System (AB2000) received FDA 510(k) clearance on 2024-09-30, under 510(k) number K241952.
Who is the listed applicant for AQUABEAM Robotic System (AB2000)?
The FDA 510(k) record lists Procept Biorobotics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AQUABEAM Robotic System (AB2000)?
The FDA product code for AQUABEAM Robotic System (AB2000) is PZP.
相關臨床試驗
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其他以 Procept Biorobotics 為申請人之記錄
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：PZP）
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。
K260723HYDROS機器人系統（HY1000）；HYDROS手持式工具（HH1000）；HYDROS TRUS 探頭（HU1000）Procept BioroboticsK253211AQUABEAM Robotic SystemProcept BioroboticsK251082HYDROS機器人系統（HY1000）；HYDROS手持式工具（HH1000）；HYDROS TRUS 探頭（HU1000）Procept BioroboticsK240200HYDROS機器人系統；HYDROS TRUS探針；HYDROS手持式工具Procept BioroboticsK231024AquaBeam 閃電系統Procept Biorobotics, CorporationK212835AquaBeam 閃電系統Procept Biorobotics, Corporation
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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