FDA 510(k)

LVIS神经匹配

K号: K222450 · 2023-06-09

决定日期2023-06-09

产品代码OMB

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决定实质等同

器械摘要

LVIS NeuroMatch is the device name listed in this FDA 510(k) record. The listed applicant is LVIS Corporation. It received FDA 510(k) clearance on 2023-06-09 under 510(k) number K222450. The device is classified under product code OMB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LVIS NeuroMatch?

LVIS NeuroMatch is a medical device that received FDA 510(k) clearance on 2023-06-09. The listed applicant is LVIS Corporation. The 510(k) number is K222450.

When did LVIS NeuroMatch receive FDA 510(k) clearance?

LVIS NeuroMatch received FDA 510(k) clearance on 2023-06-09, under 510(k) number K222450.

Who is the listed applicant for LVIS NeuroMatch?

The FDA 510(k) record lists LVIS Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LVIS NeuroMatch?

The FDA product code for LVIS NeuroMatch is OMB.

列明LVIS Corporation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。

K250239NeuroMatch K241390NeuroMatch

官方来源

在 FDA 数据库中查看 →

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