双模式移动C-臂（Geelin500A，Geelin500M）
K号: K251004 · 2025-11-06
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器械摘要
Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M) is the device name listed in this FDA 510(k) record. The listed applicant is Hefei Chimed Intelligent Machine Co., Ltd.. It received FDA 510(k) clearance on 2025-11-06 under 510(k) number K251004. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M)?
Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M) is a medical device that received FDA 510(k) clearance on 2025-11-06. The listed applicant is Hefei Chimed Intelligent Machine Co., Ltd.. The 510(k) number is K251004.
When did Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M) receive FDA 510(k) clearance?
Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M) received FDA 510(k) clearance on 2025-11-06, under 510(k) number K251004.
Who is the listed applicant for Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M)?
The FDA 510(k) record lists Hefei Chimed Intelligent Machine Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M)?
The FDA product code for Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M) is OXO.
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。
相关器械（代码：OXO）
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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