智能同步
K号: K212271 · 2022-02-04
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器械摘要
smart-sync is the device name listed in this FDA 510(k) record. The listed applicant is Northh Medical GmbH. It received FDA 510(k) clearance on 2022-02-04 under 510(k) number K212271. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the smart-sync?
smart-sync is a medical device that received FDA 510(k) clearance on 2022-02-04. The listed applicant is Northh Medical GmbH. The 510(k) number is K212271.
When did smart-sync receive FDA 510(k) clearance?
smart-sync received FDA 510(k) clearance on 2022-02-04, under 510(k) number K212271.
Who is the listed applicant for smart-sync?
The FDA 510(k) record lists Northh Medical GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for smart-sync?
The FDA product code for smart-sync is LNH.
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：LNH）
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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