超能凝胶
K号: K211691 · 2021-12-22
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器械摘要
Ultrast Gel is the device name listed in this FDA 510(k) record. The listed applicant is Ultrast, Inc.. It received FDA 510(k) clearance on 2021-12-22 under 510(k) number K211691. The device is classified under product code MUI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Ultrast Gel?
Ultrast Gel is a medical device that received FDA 510(k) clearance on 2021-12-22. The listed applicant is Ultrast, Inc.. The 510(k) number is K211691.
When did Ultrast Gel receive FDA 510(k) clearance?
Ultrast Gel received FDA 510(k) clearance on 2021-12-22, under 510(k) number K211691.
Who is the listed applicant for Ultrast Gel?
The FDA 510(k) record lists Ultrast, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ultrast Gel?
The FDA product code for Ultrast Gel is MUI.
相关临床试验
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相关器械（代码：MUI）
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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