FDA 510(k)

二极管激光治疗系统（V19）

K号: K260307 · 2026-04-15

申请人Weifang Mingliang Electronics Co., Ltd.

决定日期2026-04-15

产品代码GEX

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决定实质等同

器械摘要

Diode Laser Therapy Systems (V19) is the device name listed in this FDA 510(k) record. The listed applicant is Weifang Mingliang Electronics Co., Ltd.. It received FDA 510(k) clearance on 2026-04-15 under 510(k) number K260307. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常见问题

What is the Diode Laser Therapy Systems (V19)?

Diode Laser Therapy Systems (V19) is a medical device that received FDA 510(k) clearance on 2026-04-15. The listed applicant is Weifang Mingliang Electronics Co., Ltd.. The 510(k) number is K260307.

When did Diode Laser Therapy Systems (V19) receive FDA 510(k) clearance?

Diode Laser Therapy Systems (V19) received FDA 510(k) clearance on 2026-04-15, under 510(k) number K260307.

Who is the listed applicant for Diode Laser Therapy Systems (V19)?

The FDA 510(k) record lists Weifang Mingliang Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Diode Laser Therapy Systems (V19)?

The FDA product code for Diode Laser Therapy Systems (V19) is GEX. This falls under the Gastroenterology category.

列明Weifang Mingliang Electronics 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。

K242183Fractional CO2 Laser Therapy System (EXFU CO2)K200525医疗二极管激光脱毛系统

官方来源

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