FDA 510(k)

Sirius MRI标记NS

K号: K171487 · 2017-08-25

决定日期2017-08-25

产品代码KXK

咨询委员会RA

决定实质等同

器械摘要

Sirius MRI Marker NS is the device name listed in this FDA 510(k) record. The listed applicant is C4 Imaging, LLC. It received FDA 510(k) clearance on 2017-08-25 under 510(k) number K171487. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sirius MRI Marker NS?

Sirius MRI Marker NS is a medical device that received FDA 510(k) clearance on 2017-08-25. The listed applicant is C4 Imaging, LLC. The 510(k) number is K171487.

When did Sirius MRI Marker NS receive FDA 510(k) clearance?

Sirius MRI Marker NS received FDA 510(k) clearance on 2017-08-25, under 510(k) number K171487.

Who is the listed applicant for Sirius MRI Marker NS?

The FDA 510(k) record lists C4 Imaging, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sirius MRI Marker NS?

The FDA product code for Sirius MRI Marker NS is KXK.

列明C4 Imaging, LLC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。

K192771C4 标记物 K180069HDR MRI腔内标记

官方来源

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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。