FDA 510(k)

Evidence MultiSTAT DOA尿液多联检测

K号: K221550 · 2023-10-05

决定日期2023-10-05

产品代码DJG

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决定实质等同

器械摘要

Evidence MultiSTAT DOA Urine MultiPlex is the device name listed in this FDA 510(k) record. The listed applicant is Randox Laboratories Limited. It received FDA 510(k) clearance on 2023-10-05 under 510(k) number K221550. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Evidence MultiSTAT DOA Urine MultiPlex?

Evidence MultiSTAT DOA Urine MultiPlex is a medical device that received FDA 510(k) clearance on 2023-10-05. The listed applicant is Randox Laboratories Limited. The 510(k) number is K221550.

When did Evidence MultiSTAT DOA Urine MultiPlex receive FDA 510(k) clearance?

Evidence MultiSTAT DOA Urine MultiPlex received FDA 510(k) clearance on 2023-10-05, under 510(k) number K221550.

Who is the listed applicant for Evidence MultiSTAT DOA Urine MultiPlex?

The FDA 510(k) record lists Randox Laboratories Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Evidence MultiSTAT DOA Urine MultiPlex?

The FDA product code for Evidence MultiSTAT DOA Urine MultiPlex is DJG.

列明Randox Laboratories Limited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。

K250741Evidence MultiSTAT DOA尿液多联检测 K220451Evidence MultiSTAT DOA尿液多联检测，Evidence MultiSTAT K162275Randox RX Daytona Plus 碱性磷酸酶 (ALP)K161691直接低密度脂蛋白胆固醇（LDL）K152343直接胆红素 K152344总胆红素

查看所有 7 个设备 →

相关器械（代码：DJG）

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。

K252684Labcorp 芬太尼尿液视觉测试Medtox Diagnostics, Inc.K250741Evidence MultiSTAT DOA尿液多联检测Randox Laboratories Limited K253082LZI 布托啡诺 II 酶联免疫测定Lin-Zhi International, Inc.K252520SEFRIA® 水合吗啡口腔液体Immunalysis Corporation K251972Healgen® AccuFluor Fentanyl Fluorescence Immunoassay (FIA)测试套件 - 定性；Healgen® 免疫荧光分析仪 (OG-H180)Healgen Scientific,, LLC K251634LZI 芬太尼 III 酶联免疫测定Lin-Zhi International, Inc.

官方来源

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