FDA 510(k)

瓦里安灭菌箱

K号: K160021 · 2016-04-13

决定日期2016-04-13

产品代码JAQ

咨询委员会RA

决定实质等同

器械摘要

Varian Sterilization Boxes 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 2016-04-13 under 510(k) number K160021. 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 Varian Sterilization Boxes?

Varian Sterilization Boxes is a medical device that received FDA 510(k) clearance on 2016-04-13. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K160021.

When did Varian Sterilization Boxes receive FDA 510(k) clearance?

Varian Sterilization Boxes received FDA 510(k) clearance on 2016-04-13, under 510(k) number K160021.

Who is the listed applicant for Varian Sterilization Boxes?

FDA 510(k)记录中列出Varian Medical Systems, Inc.为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for Varian Sterilization Boxes?

The FDA product code for Varian Sterilization Boxes is JAQ.

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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