FDA 510(k)

Curian Campy

K号: K210976 · 2021-12-23

决定日期2021-12-23

产品代码LQP

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决定实质等同

器械摘要

Curian Campy is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Bioscience, Inc.. It received FDA 510(k) clearance on 2021-12-23 under 510(k) number K210976. The device is classified under product code LQP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Curian Campy?

Curian Campy is a medical device that received FDA 510(k) clearance on 2021-12-23. The listed applicant is Meridian Bioscience, Inc.. The 510(k) number is K210976.

When did Curian Campy receive FDA 510(k) clearance?

Curian Campy received FDA 510(k) clearance on 2021-12-23, under 510(k) number K210976.

Who is the listed applicant for Curian Campy?

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

What is the FDA product code for Curian Campy?

The FDA product code for Curian Campy is LQP.

列明Meridian Bioscience, 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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