FDA 510(k)

QUANTA Flash RF IgM 试剂，QUANTA Flash RF IgA 试剂

K号: K190088 · 2019-04-17

决定日期2019-04-17

产品代码DHR

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决定实质等同

器械摘要

QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents is the device name listed in this FDA 510(k) record. The listed applicant is Inova Diagnostics, Inc.. It received FDA 510(k) clearance on 2019-04-17 under 510(k) number K190088. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents?

QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents is a medical device that received FDA 510(k) clearance on 2019-04-17. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K190088.

When did QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents receive FDA 510(k) clearance?

QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents received FDA 510(k) clearance on 2019-04-17, under 510(k) number K190088.

Who is the listed applicant for QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents?

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

What is the FDA product code for QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents?

The FDA product code for QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents is DHR.

列明Inova Diagnostics, 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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官方来源

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