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FDA 510(k)

Heyman Packing Applicator Set

K号: K160045 · 2016-11-17

申请人Varian Medical Systems, Inc.
决定日期2016-11-17
产品代码JAQ
咨询委员会RA
决定Substantially Equivalent

器械摘要

Heyman Packing Applicator Set 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 2016-11-17 under 510(k) number K160045. 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 Heyman Packing Applicator Set?

Heyman Packing Applicator Set is a medical device that received FDA 510(k) clearance on 2016-11-17. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K160045.

When did Heyman Packing Applicator Set receive FDA 510(k) clearance?

Heyman Packing Applicator Set received FDA 510(k) clearance on 2016-11-17, under 510(k) number K160045.

Who is the listed applicant for Heyman Packing Applicator Set?

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 Heyman Packing Applicator Set?

The FDA product code for Heyman Packing Applicator Set is JAQ.

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列明Varian Medical Systems, 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。

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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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官方来源

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