FDA 510(k)

Aptiva APS IgG 试剂; Aptiva APS IgM 试剂

K号: K223093 · 2024-12-17

决定日期2024-12-17

产品代码MID

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决定实质等同

器械摘要

Aptiva APS IgG Reagent; Aptiva APS IgM Reagent 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 2024-12-17 under 510(k) number K223093. The device is classified under product code MID. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Aptiva APS IgG Reagent; Aptiva APS IgM Reagent?

Aptiva APS IgG Reagent; Aptiva APS IgM Reagent is a medical device that received FDA 510(k) clearance on 2024-12-17. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K223093.

When did Aptiva APS IgG Reagent; Aptiva APS IgM Reagent receive FDA 510(k) clearance?

Aptiva APS IgG Reagent; Aptiva APS IgM Reagent received FDA 510(k) clearance on 2024-12-17, under 510(k) number K223093.

Who is the listed applicant for Aptiva APS IgG Reagent; Aptiva APS IgM Reagent?

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 Aptiva APS IgG Reagent; Aptiva APS IgM Reagent?

The FDA product code for Aptiva APS IgG Reagent; Aptiva APS IgM Reagent is MID.

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。

K243979Aptiva APS IgA 试剂 K213403Aptiva CTD 基础试剂 K200230Aptiva 慢性炎症性肠病 IgG 试剂 K193604Aptiva 慢性炎症性肠病 IgA 试剂 K192916NOVA Lite DAPI dsDNA Crithidia luciliae试剂盒 K190088QUANTA Flash RF IgM 试剂，QUANTA Flash RF IgA 试剂

查看所有 16 个设备 →

官方来源

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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。

器械摘要

常见问题

相关临床试验

列明Inova Diagnostics, Inc.为申报人的其他记录

官方来源