UC-CARE NaviGo 工作站
K号: K160934 · 2017-02-06
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器械摘要
UC-CARE NaviGo Workstation 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 2017-02-06 under 510(k) number K160934. 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 UC-CARE NaviGo Workstation?
UC-CARE NaviGo Workstation is a medical device that received FDA 510(k) clearance on 2017-02-06. The listed applicant is UC-CARE , Ltd.. The 510(k) number is K160934.
When did UC-CARE NaviGo Workstation receive FDA 510(k) clearance?
UC-CARE NaviGo Workstation received FDA 510(k) clearance on 2017-02-06, under 510(k) number K160934.
Who is the listed applicant for UC-CARE NaviGo Workstation?
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 UC-CARE NaviGo Workstation?
The FDA product code for UC-CARE NaviGo Workstation 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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