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FDA 510(k)

Gold Standard Diagnostics 摩氏菌 VlsE-OspC IgG/IgM ELISA 测试试剂盒

K号: K203289 · 2021-03-22

决定日期2021-03-22
产品代码LSR
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器械摘要

Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit is the device name listed in this FDA 510(k) record. The listed applicant is Gold Standard Diagnostics. It received FDA 510(k) clearance on 2021-03-22 under 510(k) number K203289. 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 Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit?

Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit is a medical device that received FDA 510(k) clearance on 2021-03-22. The listed applicant is Gold Standard Diagnostics. The 510(k) number is K203289.

When did Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit receive FDA 510(k) clearance?

Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit received FDA 510(k) clearance on 2021-03-22, under 510(k) number K203289.

Who is the listed applicant for Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit?

The FDA 510(k) record lists Gold Standard Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit?

The FDA product code for Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit is LSR.

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列明Gold Standard Diagnostics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。

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