LED光疗设备
K号: K162098 · 2017-01-30
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器械摘要
常见问题
What is the LED Phototherapy Device?
LED Phototherapy Device is a medical device that received FDA 510(k) clearance on 2017-01-30. The listed applicant is Li-Tek Electronic Technology Corporation. The 510(k) number is K162098.
When did LED Phototherapy Device receive FDA 510(k) clearance?
LED Phototherapy Device received FDA 510(k) clearance on 2017-01-30, under 510(k) number K162098.
Who is the listed applicant for LED Phototherapy Device?
The FDA 510(k) record lists Li-Tek Electronic Technology Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LED Phototherapy Device?
The FDA product code for LED Phototherapy Device is OLP.
相关临床试验
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列明Li-Tek Electronic Technology Corporation为申报人的其他记录
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。
相关器械(代码:OLP)
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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