FDA 510(k)

PercuNav图像融合和介入导航

K号: K170716 · 2017-04-21

决定日期2017-04-21

产品代码JAK

咨询委员会RA

决定实质等同

器械摘要

PercuNav Image Fusion and Interventional Navigation is the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, Inc.. It received FDA 510(k) clearance on 2017-04-21 under 510(k) number K170716. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the PercuNav Image Fusion and Interventional Navigation?

PercuNav Image Fusion and Interventional Navigation is a medical device that received FDA 510(k) clearance on 2017-04-21. The listed applicant is Philips Ultrasound, Inc.. The 510(k) number is K170716.

When did PercuNav Image Fusion and Interventional Navigation receive FDA 510(k) clearance?

PercuNav Image Fusion and Interventional Navigation received FDA 510(k) clearance on 2017-04-21, under 510(k) number K170716.

Who is the listed applicant for PercuNav Image Fusion and Interventional Navigation?

The FDA 510(k) record lists Philips Ultrasound, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PercuNav Image Fusion and Interventional Navigation?

The FDA product code for PercuNav Image Fusion and Interventional Navigation is JAK.

列明Philips Ultrasound, Inc.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。

K212777Collaboration Live K203406Lumify 诊断超声系统 K200603AAA 模型 K201665Collaboration Live K202216EPIQ 系列诊断超声系统 K201053PercuNav图像融合和介入导航

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