棒棒糖咬合块
K号: K200652 · 2020-07-06
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器械摘要
Lollipop BiteBlock is the device name listed in this FDA 510(k) record. The listed applicant is Radtec Medical Devices, Inc.. It received FDA 510(k) clearance on 2020-07-06 under 510(k) number K200652. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Lollipop BiteBlock?
Lollipop BiteBlock is a medical device that received FDA 510(k) clearance on 2020-07-06. The listed applicant is Radtec Medical Devices, Inc.. The 510(k) number is K200652.
When did Lollipop BiteBlock receive FDA 510(k) clearance?
Lollipop BiteBlock received FDA 510(k) clearance on 2020-07-06, under 510(k) number K200652.
Who is the listed applicant for Lollipop BiteBlock?
The FDA 510(k) record lists Radtec Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lollipop BiteBlock?
The FDA product code for Lollipop BiteBlock is IYE.
相关临床试验
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相关器械（代码：IYE）
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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