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FDA 510(k)

Simplexa® COVID-19/流感A/B & RSV 直接检测（MOL4450）；Simplexa® COVID-19/流感A/B & RSV 阳性对照包（MOL4460）

K号: K252387 · 2025-10-30

申请人Diasorin Molecular, LLC
决定日期2025-10-30
产品代码QOF
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决定实质等同

器械摘要

Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460) is the device name listed in this FDA 510(k) record. The listed applicant is Diasorin Molecular, LLC. It received FDA 510(k) clearance on 2025-10-30 under 510(k) number K252387. The device is classified under product code QOF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460)?

Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460) is a medical device that received FDA 510(k) clearance on 2025-10-30. The listed applicant is Diasorin Molecular, LLC. The 510(k) number is K252387.

When did Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460) receive FDA 510(k) clearance?

Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460) received FDA 510(k) clearance on 2025-10-30, under 510(k) number K252387.

Who is the listed applicant for Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460)?

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

What is the FDA product code for Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460)?

The FDA product code for Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460) is QOF.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Diasorin Molecular, LLC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。

K260333LIAISON NES A组链球菌；LIAISON NES A组链球菌控制拭子套件K251978LIAISON NES 流感A/B，RSV & COVID-19K220963Simplexa COVID-19 & 流感 A/B 直接检测K202755Simplexa 先天性巨细胞病毒直接检测和Simplexa 先天性巨细胞病毒阳性对照包K212147Simplexa COVID-19 直接检测K201505Simplexa 流感 A/B & RSV 直接检测 II代，Simplexa 流感 A/B & RSV 阳性对照包

查看所有 13 个设备 →

相关器械（代码：QOF）

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。

K261336Xpert呼吸检测板CepheidK263054BIOFIRE呼吸检测板2.1（RP2.1）Biofire DiagnosticsK261837FINDER流感A&B/SARS-CoV-2测试Baebies, Inc.K252932Fast PCR Mini 呼吸检测板Autonomous Medical Devices IncorporatedK252269FINDER流感A&B/SARS-CoV-2测试Baebies, Inc.K251742VELO 呼吸测试Lex Diagnostics Limited

官方来源

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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。

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