INVU by Nuvo
K号: K210025 · 2021-05-28
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决定日期2021-05-28
产品代码LQK
咨询委员会OB
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决定实质等同
器械摘要
INVU by Nuvo is the device name listed in this FDA 510(k) record. The listed applicant is Nuvo- Group , Ltd.. It received FDA 510(k) clearance on 2021-05-28 under 510(k) number K210025. The device is classified under product code LQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the INVU by Nuvo?
INVU by Nuvo is a medical device that received FDA 510(k) clearance on 2021-05-28. The listed applicant is Nuvo- Group , Ltd.. The 510(k) number is K210025.
When did INVU by Nuvo receive FDA 510(k) clearance?
INVU by Nuvo received FDA 510(k) clearance on 2021-05-28, under 510(k) number K210025.
Who is the listed applicant for INVU by Nuvo?
The FDA 510(k) record lists Nuvo- Group , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INVU by Nuvo?
The FDA product code for INVU by Nuvo is LQK.
列明Nuvo- Group , 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：LQK）
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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