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FDA 510(k)

AUTION EYE AI-4510 尿液颗粒分析系统

K号: K232416 · 2024-05-03

申请人Arkray, Inc.
决定日期2024-05-03
产品代码LKM
咨询委员会HE 请注意,由于您只提供了“HE”作为输入,我无法提供完整的翻译。请提供完整的描述或文本,以便我能够进行准确的翻译。
决定实质等同

器械摘要

AUTION EYE AI-4510 Urine Particle Analysis System is the device name listed in this FDA 510(k) record. The listed applicant is Arkray, Inc.. It received FDA 510(k) clearance on 2024-05-03 under 510(k) number K232416. The device is classified under product code LKM. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AUTION EYE AI-4510 Urine Particle Analysis System?

AUTION EYE AI-4510 Urine Particle Analysis System is a medical device that received FDA 510(k) clearance on 2024-05-03. The listed applicant is Arkray, Inc.. The 510(k) number is K232416.

When did AUTION EYE AI-4510 Urine Particle Analysis System receive FDA 510(k) clearance?

AUTION EYE AI-4510 Urine Particle Analysis System received FDA 510(k) clearance on 2024-05-03, under 510(k) number K232416.

Who is the listed applicant for AUTION EYE AI-4510 Urine Particle Analysis System?

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

What is the FDA product code for AUTION EYE AI-4510 Urine Particle Analysis System?

The FDA product code for AUTION EYE AI-4510 Urine Particle Analysis System is LKM.

相关临床试验

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列明Arkray, Inc.为申报人的其他记录

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相关器械(代码:LKM)

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。

官方来源

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