TCL3 运动跟踪系统
K号: K221785 · 2022-08-29
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器械摘要
TCL3 Motion Tracking System is the device name listed in this FDA 510(k) record. The listed applicant is Tracinnovations A/S. It received FDA 510(k) clearance on 2022-08-29 under 510(k) number K221785. 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 TCL3 Motion Tracking System?
TCL3 Motion Tracking System is a medical device that received FDA 510(k) clearance on 2022-08-29. The listed applicant is Tracinnovations A/S. The 510(k) number is K221785.
When did TCL3 Motion Tracking System receive FDA 510(k) clearance?
TCL3 Motion Tracking System received FDA 510(k) clearance on 2022-08-29, under 510(k) number K221785.
Who is the listed applicant for TCL3 Motion Tracking System?
The FDA 510(k) record lists Tracinnovations A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TCL3 Motion Tracking System?
The FDA product code for TCL3 Motion Tracking System is LNH.
相关临床试验
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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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