INNOLUX RIC
K号: K162344 · 2016-12-20
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器械摘要
INNOLUX RIC is the device name listed in this FDA 510(k) record. The listed applicant is Innolux Corporation. It received FDA 510(k) clearance on 2016-12-20 under 510(k) number K162344. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the INNOLUX RIC?
INNOLUX RIC is a medical device that received FDA 510(k) clearance on 2016-12-20. The listed applicant is Innolux Corporation. The 510(k) number is K162344.
When did INNOLUX RIC receive FDA 510(k) clearance?
INNOLUX RIC received FDA 510(k) clearance on 2016-12-20, under 510(k) number K162344.
Who is the listed applicant for INNOLUX RIC?
The FDA 510(k) record lists Innolux Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INNOLUX RIC?
The FDA product code for INNOLUX RIC is MQB.
相关临床试验
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相关器械（代码：MQB）
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。
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官方来源
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