免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

Rapid Fentanyl (FYL) 测试条,Rapid Fentanyl (FYL) 测试浸卡

K号: K231904 · 2024-03-08

决定日期2024-03-08
产品代码DJG
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

Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard is the device name listed in this FDA 510(k) record. The listed applicant is Co-Innovation Biotech Co., Ltd.. It received FDA 510(k) clearance on 2024-03-08 under 510(k) number K231904. 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 Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard?

Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard is a medical device that received FDA 510(k) clearance on 2024-03-08. The listed applicant is Co-Innovation Biotech Co., Ltd.. The 510(k) number is K231904.

When did Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard receive FDA 510(k) clearance?

Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard received FDA 510(k) clearance on 2024-03-08, under 510(k) number K231904.

Who is the listed applicant for Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard?

The FDA 510(k) record lists Co-Innovation Biotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard?

The FDA product code for Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard is DJG.

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Co-Innovation Biotech Co., Ltd.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: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。

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。

↑