ARTHUR
K号: K260190 · 2026-06-18
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器械摘要
ARTHUR is the device name listed in this FDA 510(k) record. The listed applicant is ROPCA ApS. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K260190. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ARTHUR?
ARTHUR is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is ROPCA ApS. The 510(k) number is K260190.
When did ARTHUR receive FDA 510(k) clearance?
ARTHUR received FDA 510(k) clearance on 2026-06-18, under 510(k) number K260190.
Who is the listed applicant for ARTHUR?
FDA 510(k)记录显示，ROPCA ApS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 ARTHUR?
The FDA product code for ARTHUR is IYO.
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ROPCA ApS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：IYO）
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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