FAQ 101
K号: K222012 · 2023-04-05
广告
器械摘要
FAQ 101 is the device name listed in this FDA 510(k) record. The listed applicant is Foreo, Inc.. It received FDA 510(k) clearance on 2023-04-05 under 510(k) number K222012. The device is classified under product code PAY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the FAQ 101?
FAQ 101 is a medical device that received FDA 510(k) clearance on 2023-04-05. The listed applicant is Foreo, Inc.. The 510(k) number is K222012.
When did FAQ 101 receive FDA 510(k) clearance?
FAQ 101 received FDA 510(k) clearance on 2023-04-05, under 510(k) number K222012.
Who is the listed applicant for FAQ 101?
The FDA 510(k) record lists Foreo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FAQ 101?
The FDA product code for FAQ 101 is PAY.
列明Foreo, Inc.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：PAY）
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。
广告