富士胶片内窥镜型号EG-S100XT和VS-1000显示单元
K号: K250550 · 2026-02-17
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决定日期2026-02-17
产品代码FDS
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定实质等同
器械摘要
FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Corporation. It received FDA 510(k) clearance on 2026-02-17 under 510(k) number K250550. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit?
FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit is a medical device that received FDA 510(k) clearance on 2026-02-17. The listed applicant is Fujifilm Corporation. The 510(k) number is K250550.
When did FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit receive FDA 510(k) clearance?
FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit received FDA 510(k) clearance on 2026-02-17, under 510(k) number K250550.
Who is the listed applicant for FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit?
FDA 510(k)记录中列出富士胶片公司为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit?
The FDA product code for FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit is FDS.
相关临床试验
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。
列明Fujifilm Corporation为申报人的其他记录
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。
相关器械（代码：FDS）
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。
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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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