DUO1 和 DUO2
K号: K241649 · 2024-07-05
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决定日期2024-07-05
产品代码MUH
咨询委员会DE
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决定实质等同
器械摘要
DUO1 and DUO2 is the device name listed in this FDA 510(k) record. The listed applicant is Zinnovi, Inc.. It received FDA 510(k) clearance on 2024-07-05 under 510(k) number K241649. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DUO1 and DUO2?
DUO1 and DUO2 is a medical device that received FDA 510(k) clearance on 2024-07-05. The listed applicant is Zinnovi, Inc.. The 510(k) number is K241649.
When did DUO1 and DUO2 receive FDA 510(k) clearance?
DUO1 and DUO2 received FDA 510(k) clearance on 2024-07-05, under 510(k) number K241649.
Who is the listed applicant for DUO1 and DUO2?
The FDA 510(k) record lists Zinnovi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUO1 and DUO2?
The FDA product code for DUO1 and DUO2 is MUH.
相关器械（代码：MUH）
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
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