Sensilight Pro / 手枪式IPL
K号: K183260 · 2019-03-18
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决定日期2019-03-18
产品代码OHT
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Sensilight Pro / Pistol IPL is the device name listed in this FDA 510(k) record. The listed applicant is El Global Trade, Ltd.. It received FDA 510(k) clearance on 2019-03-18 under 510(k) number K183260. 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 Sensilight Pro / Pistol IPL?
Sensilight Pro / Pistol IPL is a medical device that received FDA 510(k) clearance on 2019-03-18. The listed applicant is El Global Trade, Ltd.. The 510(k) number is K183260.
When did Sensilight Pro / Pistol IPL receive FDA 510(k) clearance?
Sensilight Pro / Pistol IPL received FDA 510(k) clearance on 2019-03-18, under 510(k) number K183260.
Who is the listed applicant for Sensilight Pro / Pistol IPL?
The FDA 510(k) record lists El Global Trade, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sensilight Pro / Pistol IPL?
The FDA product code for Sensilight Pro / Pistol IPL is OHT.
相关临床试验
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列明El Global Trade, Ltd.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：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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