Nulife
K号: K210969 · 2021-11-03
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决定日期2021-11-03
产品代码KGO
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Nulife is the device name listed in this FDA 510(k) record. The listed applicant is Mrk Healthcare Pvt, Ltd.. It received FDA 510(k) clearance on 2021-11-03 under 510(k) number K210969. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Nulife?
Nulife is a medical device that received FDA 510(k) clearance on 2021-11-03. The listed applicant is Mrk Healthcare Pvt, Ltd.. The 510(k) number is K210969.
When did Nulife receive FDA 510(k) clearance?
Nulife received FDA 510(k) clearance on 2021-11-03, under 510(k) number K210969.
Who is the listed applicant for Nulife?
The FDA 510(k) record lists Mrk Healthcare Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nulife?
The FDA product code for Nulife is KGO.
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：KGO）
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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