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FDA 510(k)

Facet Aurora 可重复使用注射针座

K号: K232912 · 2024-01-25

决定日期2024-01-25
产品代码QRL
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

Facet Aurora Reusable Lancet Base is the device name listed in this FDA 510(k) record. The listed applicant is Facet Technologies, LLC. It received FDA 510(k) clearance on 2024-01-25 under 510(k) number K232912. The device is classified under product code QRL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Facet Aurora Reusable Lancet Base?

Facet Aurora Reusable Lancet Base is a medical device that received FDA 510(k) clearance on 2024-01-25. The listed applicant is Facet Technologies, LLC. The 510(k) number is K232912.

When did Facet Aurora Reusable Lancet Base receive FDA 510(k) clearance?

Facet Aurora Reusable Lancet Base received FDA 510(k) clearance on 2024-01-25, under 510(k) number K232912.

Who is the listed applicant for Facet Aurora Reusable Lancet Base?

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

What is the FDA product code for Facet Aurora Reusable Lancet Base?

The FDA product code for Facet Aurora Reusable Lancet Base is QRL.

相关临床试验

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。

列明Facet Technologies, LLC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。

相关器械(代码:QRL)

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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