Urbanek 设备
K号: K170985 · 2017-09-25
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器械摘要
Urbanek Device is the device name listed in this FDA 510(k) record. The listed applicant is Tmj Services, LLC. It received FDA 510(k) clearance on 2017-09-25 under 510(k) number K170985. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.
常见问题
What is the Urbanek Device?
Urbanek Device is a medical device that received FDA 510(k) clearance on 2017-09-25. The listed applicant is Tmj Services, LLC. The 510(k) number is K170985.
When did Urbanek Device receive FDA 510(k) clearance?
Urbanek Device received FDA 510(k) clearance on 2017-09-25, under 510(k) number K170985.
Who is the listed applicant for Urbanek Device?
The FDA 510(k) record lists Tmj Services, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Urbanek Device?
The FDA product code for Urbanek Device is MQC.
相关临床试验
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相关器械（代码：MQC）
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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