双芯
K号: K260805 · 2026-05-11
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决定日期2026-05-11
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
Dual Core is the device name listed in this FDA 510(k) record. The listed applicant is Vericom Co., Ltd.. It received FDA 510(k) clearance on 2026-05-11 under 510(k) number K260805. 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 Dual Core?
Dual Core is a medical device that received FDA 510(k) clearance on 2026-05-11. The listed applicant is Vericom Co., Ltd.. The 510(k) number is K260805.
When did Dual Core receive FDA 510(k) clearance?
Dual Core received FDA 510(k) clearance on 2026-05-11, under 510(k) number K260805.
Who is the listed applicant for Dual Core?
The FDA 510(k) record lists Vericom Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dual Core?
The FDA product code for Dual Core is EBF.
列明Vericom Co., Ltd.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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