Dentilube Spray
K号: K202689 · 2021-09-03
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器械摘要
Dentilube Spray is the device name listed in this FDA 510(k) record. The listed applicant is Oxy2plus, LLC. It received FDA 510(k) clearance on 2021-09-03 under 510(k) number K202689. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.
常见问题
What is the Dentilube Spray?
Dentilube Spray is a medical device that received FDA 510(k) clearance on 2021-09-03. The listed applicant is Oxy2plus, LLC. The 510(k) number is K202689.
When did Dentilube Spray receive FDA 510(k) clearance?
Dentilube Spray received FDA 510(k) clearance on 2021-09-03, under 510(k) number K202689.
Who is the listed applicant for Dentilube Spray?
The FDA 510(k) record lists Oxy2plus, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dentilube Spray?
The FDA product code for Dentilube Spray is LFD.
相关临床试验
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相关器械（代码：LFD）
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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