Kurin血液培养收集套装带Kurin锁技术
K号: K220677 · 2023-04-28
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器械摘要
常见问题
What is the Kurin Blood Culture Collection Set with Kurin Lock Technology?
Kurin Blood Culture Collection Set with Kurin Lock Technology is a medical device that received FDA 510(k) clearance on 2023-04-28. The listed applicant is Kurin, Inc.. The 510(k) number is K220677.
When did Kurin Blood Culture Collection Set with Kurin Lock Technology receive FDA 510(k) clearance?
Kurin Blood Culture Collection Set with Kurin Lock Technology received FDA 510(k) clearance on 2023-04-28, under 510(k) number K220677.
Who is the listed applicant for Kurin Blood Culture Collection Set with Kurin Lock Technology?
The FDA 510(k) record lists Kurin, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kurin Blood Culture Collection Set with Kurin Lock Technology?
The FDA product code for Kurin Blood Culture Collection Set with Kurin Lock Technology is JKA.
相关临床试验
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列明Kurin, 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。
相关器械(代码:JKA)
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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