Cornisol
K号: K221759 · 2022-10-05
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器械摘要
Cornisol is the device name listed in this FDA 510(k) record. The listed applicant is Aurolab. It received FDA 510(k) clearance on 2022-10-05 under 510(k) number K221759. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.
常见问题
What is the Cornisol?
Cornisol is a medical device that received FDA 510(k) clearance on 2022-10-05. The listed applicant is Aurolab. The 510(k) number is K221759.
When did Cornisol receive FDA 510(k) clearance?
Cornisol received FDA 510(k) clearance on 2022-10-05, under 510(k) number K221759.
Who is the listed applicant for Cornisol?
The FDA 510(k) record lists Aurolab as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cornisol?
The FDA product code for Cornisol is LYX.
相关临床试验
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相关器械（代码：LYX）
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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