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FDA 510(k)

Advanced Breast Template System

K号: K161540 · 2016-10-20

申请人Varian Medical Systems, Inc.
决定日期2016-10-20
产品代码JAQ
咨询委员会RA
决定Substantially Equivalent

器械摘要

Advanced Breast Template System is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2016-10-20 under 510(k) number K161540. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Advanced Breast Template System?

Advanced Breast Template System is a medical device that received FDA 510(k) clearance on 2016-10-20. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K161540.

When did Advanced Breast Template System receive FDA 510(k) clearance?

Advanced Breast Template System received FDA 510(k) clearance on 2016-10-20, under 510(k) number K161540.

Who is the listed applicant for Advanced Breast Template System?

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

What is the FDA product code for Advanced Breast Template System?

The FDA product code for Advanced Breast Template System is JAQ.

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列明Varian Medical Systems, Inc.为申报人的其他记录

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相关器械（代码：JAQ）

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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