一次性数字软性输尿管镜 (7.5F)；视频成像处理器（型号 HV-200）
K号: K252929 · 2026-04-09
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器械摘要
常见问题
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.
相关临床试验
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相关器械（代码：FGB）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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