Lucent : IPL
K号: K193072 · 2020-03-05
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决定日期2020-03-05
产品代码ONF
咨询委员会SU
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决定实质等同
器械摘要
Lucent : IPL is the device name listed in this FDA 510(k) record. The listed applicant is Luvo Medical Technologies, Inc.. It received FDA 510(k) clearance on 2020-03-05 under 510(k) number K193072. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Lucent : IPL?
Lucent : IPL is a medical device that received FDA 510(k) clearance on 2020-03-05. The listed applicant is Luvo Medical Technologies, Inc.. The 510(k) number is K193072.
When did Lucent : IPL receive FDA 510(k) clearance?
Lucent : IPL received FDA 510(k) clearance on 2020-03-05, under 510(k) number K193072.
Who is the listed applicant for Lucent : IPL?
The FDA 510(k) record lists Luvo Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lucent : IPL?
The FDA product code for Lucent : IPL is ONF.
相关临床试验
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列明Luvo Medical Technologies, 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：ONF）
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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