Facet Aurora 可重复使用注射针座
K号: K232912 · 2024-01-25
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器械摘要
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
在 FDA 数据库中查看 →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。
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