FDA 510(k)

Alere i 流感A & B，Alere i 流感A & B控制拭子套装，Alere i 仪器

K号: K163266 · 2016-12-21

决定日期2016-12-21

产品代码OCC

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决定实质等同

器械摘要

Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument 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 2016-12-21 under 510(k) number K163266. The device is classified under product code OCC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument?

Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument is a medical device that received FDA 510(k) clearance on 2016-12-21. The listed applicant is Alere Scarborough, Inc.. The 510(k) number is K163266.

When did Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument receive FDA 510(k) clearance?

Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument received FDA 510(k) clearance on 2016-12-21, under 510(k) number K163266.

Who is the listed applicant for Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument?

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 Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument?

The FDA product code for Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument is OCC.

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。

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