平面LED支架
K号: K230362 · 2023-09-11
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决定日期2023-09-11
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
Planar LED mate is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Leaflife Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-09-11 under 510(k) number K230362. 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 Planar LED mate?
Planar LED mate is a medical device that received FDA 510(k) clearance on 2023-09-11. The listed applicant is Shenzhen Leaflife Technology Co., Ltd.. The 510(k) number is K230362.
When did Planar LED mate receive FDA 510(k) clearance?
Planar LED mate received FDA 510(k) clearance on 2023-09-11, under 510(k) number K230362.
Who is the listed applicant for Planar LED mate?
The FDA 510(k) record lists Shenzhen Leaflife Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Planar LED mate?
The FDA product code for Planar LED mate 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。
列明Shenzhen Leaflife Technology Co., 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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