IPL脱毛设备
K号: K232274 · 2023-09-28
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器械摘要
IPL hair removal device is the device name listed in this FDA 510(k) record. The listed applicant is Lumenessa Corp. It received FDA 510(k) clearance on 2023-09-28 under 510(k) number K232274. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the IPL hair removal device?
IPL hair removal device is a medical device that received FDA 510(k) clearance on 2023-09-28. The listed applicant is Lumenessa Corp. The 510(k) number is K232274.
When did IPL hair removal device receive FDA 510(k) clearance?
IPL hair removal device received FDA 510(k) clearance on 2023-09-28, under 510(k) number K232274.
Who is the listed applicant for IPL hair removal device?
The FDA 510(k) record lists Lumenessa Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IPL hair removal device?
The FDA product code for IPL hair removal device is OHT.
相关临床试验
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：OHT）
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。
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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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