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FDA 510(k)

KBL太阳灯产品(=设备捆绑名称)

K号: K151962 · 2016-09-15

申请人Kbl AG
决定日期2016-09-15
产品代码LEJ
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

KBL Sunlamp Products (= Device Bundling name) is the device name listed in this FDA 510(k) record. The listed applicant is Kbl AG. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K151962. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the KBL Sunlamp Products (= Device Bundling name)?

KBL Sunlamp Products (= Device Bundling name) is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Kbl AG. The 510(k) number is K151962.

When did KBL Sunlamp Products (= Device Bundling name) receive FDA 510(k) clearance?

KBL Sunlamp Products (= Device Bundling name) received FDA 510(k) clearance on 2016-09-15, under 510(k) number K151962.

Who is the listed applicant for KBL Sunlamp Products (= Device Bundling name)?

The FDA 510(k) record lists Kbl AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KBL Sunlamp Products (= Device Bundling name)?

The FDA product code for KBL Sunlamp Products (= Device Bundling name) is LEJ.

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。

相关器械(代码:LEJ)

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

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