單次使用吸引-排空輸尿管進入鞘
K 號:K250128 · 2025-09-19
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器材摘要
常見問題
What is the Single Use Suction-Evacuation Ureteral Access Sheath?
Single Use Suction-Evacuation Ureteral Access Sheath is a medical device that received FDA 510(k) clearance on 2025-09-19. The listed applicant is Anhui Happiness Workshop Medical Instruments Co., Ltd.. The 510(k) number is K250128.
When did Single Use Suction-Evacuation Ureteral Access Sheath receive FDA 510(k) clearance?
Single Use Suction-Evacuation Ureteral Access Sheath received FDA 510(k) clearance on 2025-09-19, under 510(k) number K250128.
Who is the listed applicant for Single Use Suction-Evacuation Ureteral Access Sheath?
The FDA 510(k) record lists Anhui Happiness Workshop Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Single Use Suction-Evacuation Ureteral Access Sheath?
The FDA product code for Single Use Suction-Evacuation Ureteral Access Sheath is FED.
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相關器械(代碼:FED)
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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