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FDA 510(k)

FIJI SUN荧光晒黑单元

K号: K151721 · 2018-06-22

决定日期2018-06-22
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

FIJI SUN FLUORESCENT TANNING UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Kdb Inc. (Dba) Sperti Sunlamp. It received FDA 510(k) clearance on 2018-06-22 under 510(k) number K151721. 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 FIJI SUN FLUORESCENT TANNING UNIT?

FIJI SUN FLUORESCENT TANNING UNIT is a medical device that received FDA 510(k) clearance on 2018-06-22. The listed applicant is Kdb Inc. (Dba) Sperti Sunlamp. The 510(k) number is K151721.

When did FIJI SUN FLUORESCENT TANNING UNIT receive FDA 510(k) clearance?

FIJI SUN FLUORESCENT TANNING UNIT received FDA 510(k) clearance on 2018-06-22, under 510(k) number K151721.

Who is the listed applicant for FIJI SUN FLUORESCENT TANNING UNIT?

The FDA 510(k) record lists Kdb Inc. (Dba) Sperti Sunlamp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIJI SUN FLUORESCENT TANNING UNIT?

The FDA product code for FIJI SUN FLUORESCENT TANNING UNIT is LEJ.

相关临床试验

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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。

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