G-CAM
K号: K220329 · 2022-08-16
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决定日期2022-08-16
产品代码EBF
咨询委员会DE
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决定实质等同
器械摘要
G-CAM is the device name listed in this FDA 510(k) record. The listed applicant is Graphenano Dental S.L.. It received FDA 510(k) clearance on 2022-08-16 under 510(k) number K220329. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the G-CAM?
G-CAM is a medical device that received FDA 510(k) clearance on 2022-08-16. The listed applicant is Graphenano Dental S.L.. The 510(k) number is K220329.
When did G-CAM receive FDA 510(k) clearance?
G-CAM received FDA 510(k) clearance on 2022-08-16, under 510(k) number K220329.
Who is the listed applicant for G-CAM?
The FDA 510(k) record lists Graphenano Dental S.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for G-CAM?
The FDA product code for G-CAM is EBF.
列明Graphenano Dental S.L.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：EBF）
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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