VEGA眼科成像与引导系统（VF-VIS-002）
K号: K260885 · 2026-06-15
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器械摘要
VERAFEYE Imaging and Guidance System (VF-VIS-002) is the device name listed in this FDA 510(k) record. The listed applicant is Luma Vision Limited. It received FDA 510(k) clearance on 2026-06-15 under 510(k) number K260885. FDA Decision: Substantially Equivalent.
常见问题
What is the VERAFEYE Imaging and Guidance System (VF-VIS-002)?
VERAFEYE Imaging and Guidance System (VF-VIS-002) is a medical device that received FDA 510(k) clearance on 2026-06-15. The listed applicant is Luma Vision Limited. The 510(k) number is K260885.
When did VERAFEYE Imaging and Guidance System (VF-VIS-002) receive FDA 510(k) clearance?
VERAFEYE Imaging and Guidance System (VF-VIS-002) received FDA 510(k) clearance on 2026-06-15, under 510(k) number K260885.
Who is the listed applicant for VERAFEYE Imaging and Guidance System (VF-VIS-002)?
FDA 510(k)记录显示Luma Vision Limited为申请人。这本身并不能确立该设备的制造商。
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Luma Vision Limited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。
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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