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FDA 510(k)

單次使用數位柔軟輸尿管鏡（7.5F）；視鏡影像處理器（型號 HV-200）

K 號：K252929 · 2026-04-09

申請人Anhui Happiness Workshop Instruments Co., Ltd.
決定日期2026-04-09
產品代碼FGB
諮詢委員會GU
決定相當於

器材摘要

Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model HV-200) is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Happiness Workshop Instruments Co., Ltd.. It received FDA 510(k) clearance on 2026-04-09 under 510(k) number K252929. The device is classified under product code FGB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model HV-200)?

Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model HV-200) is a medical device that received FDA 510(k) clearance on 2026-04-09. The listed applicant is Anhui Happiness Workshop Instruments Co., Ltd.. The 510(k) number is K252929.

When did Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model HV-200) receive FDA 510(k) clearance?

Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model HV-200) received FDA 510(k) clearance on 2026-04-09, under 510(k) number K252929.

Who is the listed applicant for Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model HV-200)?

The FDA 510(k) record lists Anhui Happiness Workshop Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model HV-200)?

The FDA product code for Single Use Digital Flexible Ureteroscope (7.5F); Videoscope Imaging Processor (Model HV-200) is FGB.

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。

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相關器械（代碼：FGB）

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

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