FDA 510(k)

StarGuide

K号: K210173 · 2021-03-29

决定日期2021-03-29

产品代码KPS

咨询委员会RA

决定实质等同

器械摘要

StarGuide is the device name listed in this FDA 510(k) record. The listed applicant is GE Healthcare. It received FDA 510(k) clearance on 2021-03-29 under 510(k) number K210173. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the StarGuide?

StarGuide is a medical device that received FDA 510(k) clearance on 2021-03-29. The listed applicant is GE Healthcare. The 510(k) number is K210173.

When did StarGuide receive FDA 510(k) clearance?

StarGuide received FDA 510(k) clearance on 2021-03-29, under 510(k) number K210173.

Who is the listed applicant for StarGuide?

The FDA 510(k) record lists GE Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for StarGuide?

The FDA product code for StarGuide is KPS.

列明GE Healthcare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。

K253639查看此医疗设备监管文本： View the medical-device regulatory text for this device_name.K242925MR Contour DL K232346数字专家访问与远程扫描 K223212Precision DL K221680Xeleris V 处理与审查系统 K221932Omni 传奇

查看所有 55 个设备 →

相关器械（代码：KPS）

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

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