FDA 510(k)

Sony IP 转换器 NU-IP40S

K号: K161122 · 2016-06-08

决定日期2016-06-08

产品代码GCJ

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决定实质等同

器械摘要

Sony IP Converter NU-IP40S is the device name listed in this FDA 510(k) record. The listed applicant is Sony Electronics, Inc.. It received FDA 510(k) clearance on 2016-06-08 under 510(k) number K161122. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sony IP Converter NU-IP40S?

Sony IP Converter NU-IP40S is a medical device that received FDA 510(k) clearance on 2016-06-08. The listed applicant is Sony Electronics, Inc.. The 510(k) number is K161122.

When did Sony IP Converter NU-IP40S receive FDA 510(k) clearance?

Sony IP Converter NU-IP40S received FDA 510(k) clearance on 2016-06-08, under 510(k) number K161122.

Who is the listed applicant for Sony IP Converter NU-IP40S?

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

What is the FDA product code for Sony IP Converter NU-IP40S?

The FDA product code for Sony IP Converter NU-IP40S is GCJ.

列明Sony Electronics, 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。

K191678IP转换器

相关器械（代码：GCJ）

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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