Navigo工作站版本2.0
K号: K173054 · 2018-01-16
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器械摘要
Navigo Workstation Version 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is UC-CARE , Ltd.. It received FDA 510(k) clearance on 2018-01-16 under 510(k) number K173054. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Navigo Workstation Version 2.0?
Navigo Workstation Version 2.0 is a medical device that received FDA 510(k) clearance on 2018-01-16. The listed applicant is UC-CARE , Ltd.. The 510(k) number is K173054.
When did Navigo Workstation Version 2.0 receive FDA 510(k) clearance?
Navigo Workstation Version 2.0 received FDA 510(k) clearance on 2018-01-16, under 510(k) number K173054.
Who is the listed applicant for Navigo Workstation Version 2.0?
FDA 510(k)记录将UC-CARE，Ltd.列为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for Navigo Workstation Version 2.0?
The FDA product code for Navigo Workstation Version 2.0 is LLZ.
相关临床试验
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列明UC-CARE , Ltd.为申报人的其他记录
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相关器械（代码：LLZ）
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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