FDA 510(k)

EchoGlo 针

K号: K171968 · 2018-01-25

决定日期2018-01-25

产品代码BSP

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决定实质等同

器械摘要

EchoGlo Needle is the device name listed in this FDA 510(k) record. The listed applicant is Smiths Medical Asd, Inc.. It received FDA 510(k) clearance on 2018-01-25 under 510(k) number K171968. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the EchoGlo Needle?

EchoGlo Needle is a medical device that received FDA 510(k) clearance on 2018-01-25. The listed applicant is Smiths Medical Asd, Inc.. The 510(k) number is K171968.

When did EchoGlo Needle receive FDA 510(k) clearance?

EchoGlo Needle received FDA 510(k) clearance on 2018-01-25, under 510(k) number K171968.

Who is the listed applicant for EchoGlo Needle?

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

What is the FDA product code for EchoGlo Needle?

The FDA product code for EchoGlo Needle is BSP.

列明Smiths Medical Asd, 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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