HD攝影鏡頭 OLYMPUS CH-S200-08-LB
K 號：K261260 · 2026-06-24
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器材摘要
HD Camera Head OLYMPUS CH-S200-08-LB is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corporation. It received FDA 510(k) clearance on 2026-06-24 under 510(k) number K261260. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the HD Camera Head OLYMPUS CH-S200-08-LB?
HD Camera Head OLYMPUS CH-S200-08-LB is a medical device that received FDA 510(k) clearance on 2026-06-24. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K261260.
When did HD Camera Head OLYMPUS CH-S200-08-LB receive FDA 510(k) clearance?
HD Camera Head OLYMPUS CH-S200-08-LB received FDA 510(k) clearance on 2026-06-24, under 510(k) number K261260.
Who is the listed applicant for HD Camera Head OLYMPUS CH-S200-08-LB?
FDA 510(k) 記錄中將Olympus Medical Systems Corporation列為申請人。這並不單獨確立該設備製造商。
What is the FDA product code for HD Camera Head OLYMPUS CH-S200-08-LB?
The FDA product code for HD Camera Head OLYMPUS CH-S200-08-LB is FET.
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。
其他以 Olympus Medical Systems Corporation 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：FET）
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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