INNOVERSE導航儀器
K 號：K241082 · 2024-06-14
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器材摘要
INNOVERSE Navigation Instruments is the device name listed in this FDA 510(k) record. The listed applicant is Innosys Co., Ltd.. It received FDA 510(k) clearance on 2024-06-14 under 510(k) number K241082. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the INNOVERSE Navigation Instruments?
INNOVERSE Navigation Instruments is a medical device that received FDA 510(k) clearance on 2024-06-14. The listed applicant is Innosys Co., Ltd.. The 510(k) number is K241082.
When did INNOVERSE Navigation Instruments receive FDA 510(k) clearance?
INNOVERSE Navigation Instruments received FDA 510(k) clearance on 2024-06-14, under 510(k) number K241082.
Who is the listed applicant for INNOVERSE Navigation Instruments?
The FDA 510(k) record lists Innosys Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INNOVERSE Navigation Instruments?
The FDA product code for INNOVERSE Navigation Instruments is OLO.
相關臨床試驗
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其他以 Innosys Co., Ltd. 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：OLO）
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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