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)

BD Veritor System for Rapid Detection of Flu A + B 实验室套装

K号: K160164 · 2016-02-25

决定日期2016-02-25
产品代码PSZ
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

BD Veritor System for Rapid Detection of Flu A + B Labratory Kit is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson & CO. It received FDA 510(k) clearance on 2016-02-25 under 510(k) number K160164. The device is classified under product code PSZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD Veritor System for Rapid Detection of Flu A + B Labratory Kit?

BD Veritor System for Rapid Detection of Flu A + B Labratory Kit is a medical device that received FDA 510(k) clearance on 2016-02-25. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K160164.

When did BD Veritor System for Rapid Detection of Flu A + B Labratory Kit receive FDA 510(k) clearance?

BD Veritor System for Rapid Detection of Flu A + B Labratory Kit received FDA 510(k) clearance on 2016-02-25, under 510(k) number K160164.

Who is the listed applicant for BD Veritor System for Rapid Detection of Flu A + B Labratory Kit?

The FDA 510(k) record lists Becton, Dickinson & CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Veritor System for Rapid Detection of Flu A + B Labratory Kit?

The FDA product code for BD Veritor System for Rapid Detection of Flu A + B Labratory Kit is PSZ.

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Becton, Dickinson & CO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:PSZ)

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。

↑