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FDA 510(k)

AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test

K号: K234006 · 2024-03-21

申请人Allsource Screening Solutions
决定日期2024-03-21
产品代码NGL
咨询委员会TX 请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test is the device name listed in this FDA 510(k) record. The listed applicant is Allsource Screening Solutions. It received FDA 510(k) clearance on 2024-03-21 under 510(k) number K234006. The device is classified under product code NGL. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test?

AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test is a medical device that received FDA 510(k) clearance on 2024-03-21. The listed applicant is Allsource Screening Solutions. The 510(k) number is K234006.

When did AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test receive FDA 510(k) clearance?

AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test received FDA 510(k) clearance on 2024-03-21, under 510(k) number K234006.

Who is the listed applicant for AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test?

The FDA 510(k) record lists Allsource Screening Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test?

The FDA product code for AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test is NGL.

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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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