FDA 510(k)

BinaxNOW G6PD 测试

K号: K161364 · 2016-06-17

决定日期2016-06-17

产品代码JBF

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决定实质等同

器械摘要

BinaxNOW G6PD Test is the device name listed in this FDA 510(k) record. The listed applicant is Alere Scarborough, Inc.. It received FDA 510(k) clearance on 2016-06-17 under 510(k) number K161364. The device is classified under product code JBF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BinaxNOW G6PD Test?

BinaxNOW G6PD Test is a medical device that received FDA 510(k) clearance on 2016-06-17. The listed applicant is Alere Scarborough, Inc.. The 510(k) number is K161364.

When did BinaxNOW G6PD Test receive FDA 510(k) clearance?

BinaxNOW G6PD Test received FDA 510(k) clearance on 2016-06-17, under 510(k) number K161364.

Who is the listed applicant for BinaxNOW G6PD Test?

The FDA 510(k) record lists Alere Scarborough, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BinaxNOW G6PD Test?

The FDA product code for BinaxNOW G6PD Test is JBF.

列明Alere Scarborough, Inc.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。

K190204ID NOW 流感A & B 2 K181853Alere BinaxNOW流感A & B卡2，Alere Reader K173653Alere i 链球菌A 2，Alere i 仪器，Alere i 链球菌A 2控制拭子套装 K173932Alere i 流感A & B，Alere i 链球菌A，Alere i RSV，Alere i 流感A & B 2 K173502Alere BinaxNOW流感A & B卡2，Alere Reader，Alere BinaxNOW流感A & B卡2控制拭子套装 K171792Alere i 流感A & B 2，Alere i 仪器，Alere i 流感A & B控制拭子套装

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