CoLumbo
K号: K220497 · 2022-06-23
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器械摘要
CoLumbo is the device name listed in this FDA 510(k) record. The listed applicant is Smart Soft Healthcare AD. It received FDA 510(k) clearance on 2022-06-23 under 510(k) number K220497. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CoLumbo?
CoLumbo is a medical device that received FDA 510(k) clearance on 2022-06-23. The listed applicant is Smart Soft Healthcare AD. The 510(k) number is K220497.
When did CoLumbo receive FDA 510(k) clearance?
CoLumbo received FDA 510(k) clearance on 2022-06-23, under 510(k) number K220497.
Who is the listed applicant for CoLumbo?
The FDA 510(k) record lists Smart Soft Healthcare AD as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CoLumbo?
The FDA product code for CoLumbo is QIH.
相关临床试验
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列明Smart Soft Healthcare AD为申报人的其他记录
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相关器械（代码：QIH）
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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