i2轮廓
K号: K233822 · 2024-08-08
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器械摘要
i2Contour is the device name listed in this FDA 510(k) record. The listed applicant is Mrimath, LLC. It received FDA 510(k) clearance on 2024-08-08 under 510(k) number K233822. 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 i2Contour?
i2Contour is a medical device that received FDA 510(k) clearance on 2024-08-08. The listed applicant is Mrimath, LLC. The 510(k) number is K233822.
When did i2Contour receive FDA 510(k) clearance?
i2Contour received FDA 510(k) clearance on 2024-08-08, under 510(k) number K233822.
Who is the listed applicant for i2Contour?
The FDA 510(k) record lists Mrimath, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for i2Contour?
The FDA product code for i2Contour is QIH.
相关临床试验
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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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