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FDA 510(k)

LIAISON 疟原虫IgM,LIAISON 疟原虫IgM控制套件,LIAISON 疟原虫总抗体加

K号: K202573 · 2021-02-18

决定日期2021-02-18
产品代码LSR
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决定实质等同

器械摘要

LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus is the device name listed in this FDA 510(k) record. The listed applicant is DiaSorin, Inc.. It received FDA 510(k) clearance on 2021-02-18 under 510(k) number K202573. The device is classified under product code LSR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus?

LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus is a medical device that received FDA 510(k) clearance on 2021-02-18. The listed applicant is DiaSorin, Inc.. The 510(k) number is K202573.

When did LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus receive FDA 510(k) clearance?

LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus received FDA 510(k) clearance on 2021-02-18, under 510(k) number K202573.

Who is the listed applicant for LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus?

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

What is the FDA product code for LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus?

The FDA product code for LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody Plus is LSR.

相关临床试验

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列明DiaSorin, Inc.为申报人的其他记录

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相关器械(代码:LSR)

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。

官方来源

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