TMJ放松
K号: K202523 · 2021-06-24
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器械摘要
TMJ Relax is the device name listed in this FDA 510(k) record. The listed applicant is Moonwalker Innovations, Inc.. It received FDA 510(k) clearance on 2021-06-24 under 510(k) number K202523. The device is classified under product code OCO. FDA Decision: Substantially Equivalent.
常见问题
What is the TMJ Relax?
TMJ Relax is a medical device that received FDA 510(k) clearance on 2021-06-24. The listed applicant is Moonwalker Innovations, Inc.. The 510(k) number is K202523.
When did TMJ Relax receive FDA 510(k) clearance?
TMJ Relax received FDA 510(k) clearance on 2021-06-24, under 510(k) number K202523.
Who is the listed applicant for TMJ Relax?
The FDA 510(k) record lists Moonwalker Innovations, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TMJ Relax?
The FDA product code for TMJ Relax is OCO.
相关临床试验
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相关器械（代码：OCO）
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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