家用脱毛设备,型号:Precise Touch Pro
K号: K213830 · 2022-02-01
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器械摘要
常见问题
What is the Home use hair removal device, model: Precise Touch Pro?
Home use hair removal device, model: Precise Touch Pro is a medical device that received FDA 510(k) clearance on 2022-02-01. The listed applicant is Iluminage Beauty Co., Limited. The 510(k) number is K213830.
When did Home use hair removal device, model: Precise Touch Pro receive FDA 510(k) clearance?
Home use hair removal device, model: Precise Touch Pro received FDA 510(k) clearance on 2022-02-01, under 510(k) number K213830.
Who is the listed applicant for Home use hair removal device, model: Precise Touch Pro?
The FDA 510(k) record lists Iluminage Beauty Co., Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Home use hair removal device, model: Precise Touch Pro?
The FDA product code for Home use hair removal device, model: Precise Touch Pro is OHT.
相关临床试验
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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。
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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