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FDA 510(k)

强脉冲光治疗仪

K号: K232932 · 2023-12-04

决定日期2023-12-04
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

Intense Pulse Light Therapeutic Apparatus is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Greatro Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-12-04 under 510(k) number K232932. 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 Intense Pulse Light Therapeutic Apparatus?

Intense Pulse Light Therapeutic Apparatus is a medical device that received FDA 510(k) clearance on 2023-12-04. The listed applicant is Shenzhen Greatro Electronic Technology Co., Ltd.. The 510(k) number is K232932.

When did Intense Pulse Light Therapeutic Apparatus receive FDA 510(k) clearance?

Intense Pulse Light Therapeutic Apparatus received FDA 510(k) clearance on 2023-12-04, under 510(k) number K232932.

Who is the listed applicant for Intense Pulse Light Therapeutic Apparatus?

The FDA 510(k) record lists Shenzhen Greatro Electronic Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intense Pulse Light Therapeutic Apparatus?

The FDA product code for Intense Pulse Light Therapeutic Apparatus is OHT.

相关临床试验

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列明Shenzhen Greatro Electronic 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。

官方来源

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