The POD
K号: K182820 · 2019-07-17
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器械摘要
The POD is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Facialdontics, LLC. It received FDA 510(k) clearance on 2019-07-17 under 510(k) number K182820. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.
常见问题
What is the The POD?
The POD is a medical device that received FDA 510(k) clearance on 2019-07-17. The listed applicant is Advanced Facialdontics, LLC. The 510(k) number is K182820.
When did The POD receive FDA 510(k) clearance?
The POD received FDA 510(k) clearance on 2019-07-17, under 510(k) number K182820.
Who is the listed applicant for The POD?
The FDA 510(k) record lists Advanced Facialdontics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for The POD?
The FDA product code for The POD is MQC.
列明Advanced Facialdontics, LLC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：MQC）
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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