Nano-Check™ COVID-19抗原测试
K号: K231187 · 2024-01-23
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决定日期2024-01-23
产品代码QVF
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器械摘要
Nano-Check™ COVID-19 Antigen Test is the device name listed in this FDA 510(k) record. The listed applicant is Nano-Ditech Corporation. It received FDA 510(k) clearance on 2024-01-23 under 510(k) number K231187. The device is classified under product code QVF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Nano-Check™ COVID-19 Antigen Test?
Nano-Check™ COVID-19 Antigen Test is a medical device that received FDA 510(k) clearance on 2024-01-23. The listed applicant is Nano-Ditech Corporation. The 510(k) number is K231187.
When did Nano-Check™ COVID-19 Antigen Test receive FDA 510(k) clearance?
Nano-Check™ COVID-19 Antigen Test received FDA 510(k) clearance on 2024-01-23, under 510(k) number K231187.
Who is the listed applicant for Nano-Check™ COVID-19 Antigen Test?
The FDA 510(k) record lists Nano-Ditech Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nano-Check™ COVID-19 Antigen Test?
The FDA product code for Nano-Check™ COVID-19 Antigen Test is QVF.
相关临床试验
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列明Nano-Ditech Corporation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。
相关器械（代码：QVF）
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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官方来源
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