FDA 510(k)

CO2 Laser System

Número K: K200042 · 2020-06-09

RequerenteBeijing Superlaser Technology Co., Ltd.

Data da decisão2020-06-09

Código do produtoGEX

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

CO2 Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Superlaser Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-06-09 under 510(k) number K200042. 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.

Perguntas frequentes

What is the CO2 Laser System?

CO2 Laser System is a medical device that received FDA 510(k) clearance on 2020-06-09. The listed applicant is Beijing Superlaser Technology Co., Ltd.. The 510(k) number is K200042.

When did CO2 Laser System receive FDA 510(k) clearance?

CO2 Laser System received FDA 510(k) clearance on 2020-06-09, under 510(k) number K200042.

Who is the listed applicant for CO2 Laser System?

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

What is the FDA product code for CO2 Laser System?

The FDA product code for CO2 Laser System is GEX. This falls under the Gastroenterology category.

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