免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

UC-CARE NaviGo 工作站

K号: K160934 · 2017-02-06

决定日期2017-02-06
产品代码LLZ
咨询委员会RA
决定实质等同

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

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。

列明UC-CARE , Ltd.为申报人的其他记录

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: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。

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。

↑