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FDA 510(k)

ICOONE 激光医疗(也称为ICOONE 医疗激光)

K号: K211272 · 2021-06-22

决定日期2021-06-22
产品代码NUV
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

ICOONE Laser Med (also referred to as ICOONE Medical laser) is the device name listed in this FDA 510(k) record. The listed applicant is I-Tech Industries Srl. It received FDA 510(k) clearance on 2021-06-22 under 510(k) number K211272. The device is classified under product code NUV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ICOONE Laser Med (also referred to as ICOONE Medical laser)?

ICOONE Laser Med (also referred to as ICOONE Medical laser) is a medical device that received FDA 510(k) clearance on 2021-06-22. The listed applicant is I-Tech Industries Srl. The 510(k) number is K211272.

When did ICOONE Laser Med (also referred to as ICOONE Medical laser) receive FDA 510(k) clearance?

ICOONE Laser Med (also referred to as ICOONE Medical laser) received FDA 510(k) clearance on 2021-06-22, under 510(k) number K211272.

Who is the listed applicant for ICOONE Laser Med (also referred to as ICOONE Medical laser)?

The FDA 510(k) record lists I-Tech Industries Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ICOONE Laser Med (also referred to as ICOONE Medical laser)?

The FDA product code for ICOONE Laser Med (also referred to as ICOONE Medical laser) is NUV.

相关临床试验

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列明I-Tech Industries Srl为申报人的其他记录

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相关器械(代码:NUV)

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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