TRIOCLEAR 系统
K号: K193622 · 2021-07-06
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决定日期2021-07-06
产品代码NXC
咨询委员会DE
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决定实质等同
器械摘要
TRIOCLEAR System is the device name listed in this FDA 510(k) record. The listed applicant is Perfection Aligner System Hong Kong Limited. It received FDA 510(k) clearance on 2021-07-06 under 510(k) number K193622. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the TRIOCLEAR System?
TRIOCLEAR System is a medical device that received FDA 510(k) clearance on 2021-07-06. The listed applicant is Perfection Aligner System Hong Kong Limited. The 510(k) number is K193622.
When did TRIOCLEAR System receive FDA 510(k) clearance?
TRIOCLEAR System received FDA 510(k) clearance on 2021-07-06, under 510(k) number K193622.
Who is the listed applicant for TRIOCLEAR System?
The FDA 510(k) record lists Perfection Aligner System Hong Kong Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRIOCLEAR System?
The FDA product code for TRIOCLEAR System is NXC.
相关临床试验
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相关器械（代码：NXC）
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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