Erchonia CLX (型号 # CFL)
K号: K252574 · 2025-12-15
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决定日期2025-12-15
产品代码OLI
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
Erchonia CLX (Model # CFL) is the device name listed in this FDA 510(k) record. The listed applicant is Erchonia Corporation. It received FDA 510(k) clearance on 2025-12-15 under 510(k) number K252574. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Erchonia CLX (Model # CFL)?
Erchonia CLX (Model # CFL) is a medical device that received FDA 510(k) clearance on 2025-12-15. The listed applicant is Erchonia Corporation. The 510(k) number is K252574.
When did Erchonia CLX (Model # CFL) receive FDA 510(k) clearance?
Erchonia CLX (Model # CFL) received FDA 510(k) clearance on 2025-12-15, under 510(k) number K252574.
Who is the listed applicant for Erchonia CLX (Model # CFL)?
The FDA 510(k) record lists Erchonia Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Erchonia CLX (Model # CFL)?
The FDA product code for Erchonia CLX (Model # CFL) is OLI.
相关临床试验
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列明Erchonia Corporation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：OLI）
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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