Nano-Check流感+COVID-19双重测试
K号: K243561 · 2025-06-17
广告
决定日期2025-06-17
产品代码SCA
咨询委员会抱歉，您提供的内容“MI”不足以进行翻译。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同
器械摘要
Nano-Check Influenza+COVID-19 Dual 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 2025-06-17 under 510(k) number K243561. The device is classified under product code SCA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Nano-Check Influenza+COVID-19 Dual Test?
Nano-Check Influenza+COVID-19 Dual Test is a medical device that received FDA 510(k) clearance on 2025-06-17. The listed applicant is Nano-Ditech Corporation. The 510(k) number is K243561.
When did Nano-Check Influenza+COVID-19 Dual Test receive FDA 510(k) clearance?
Nano-Check Influenza+COVID-19 Dual Test received FDA 510(k) clearance on 2025-06-17, under 510(k) number K243561.
Who is the listed applicant for Nano-Check Influenza+COVID-19 Dual 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 Influenza+COVID-19 Dual Test?
The FDA product code for Nano-Check Influenza+COVID-19 Dual Test is SCA.
相关临床试验
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。
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：SCA）
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。
K261212Flowflex Plus RSV + 流感A/B + COVID快速测试ACON Laboratories, Inc.K251092iHealth 流感A&B/COVID-19 快速测试；iHealth 流感A&B/COVID-19 快速测试专业版Ihealth Labs, Inc.K251085iHealth流感A&B/COVID-19/RSV快速检测；iHealth流感A&B/COVID-19/RSV快速检测专业版Ihealth Labs, Inc.K251538Status® COVID-19/流感A&BPrinceton BioMeditech Corp.K251749Flowflex Plus RSV + Flu A/B + COVID Home TestACON Laboratories, Inc.K251604CareSuperb COVID-19/流感 A&B 抗原组合家用检测Access Bio, Inc.
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
广告