FDA 510(k)

Liger 医疗 HTU-110

K号: K152843 · 2016-06-24

决定日期2016-06-24

产品代码HGI

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决定实质等同

器械摘要

Liger Medical HTU-110 is the device name listed in this FDA 510(k) record. The listed applicant is Liger Medical, LLC. It received FDA 510(k) clearance on 2016-06-24 under 510(k) number K152843. The device is classified under product code HGI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Liger Medical HTU-110?

Liger Medical HTU-110 is a medical device that received FDA 510(k) clearance on 2016-06-24. The listed applicant is Liger Medical, LLC. The 510(k) number is K152843.

When did Liger Medical HTU-110 receive FDA 510(k) clearance?

Liger Medical HTU-110 received FDA 510(k) clearance on 2016-06-24, under 510(k) number K152843.

Who is the listed applicant for Liger Medical HTU-110?

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

What is the FDA product code for Liger Medical HTU-110?

The FDA product code for Liger Medical HTU-110 is HGI.

列明Liger Medical, LLC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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