FDA 510(k)

Co2 Laser System, Models: PureLase And VanLase

N.º K: K232133 · 2024-04-16

SolicitanteCpmt Laser (Canadian Pioneer Medical Technology Corporation)

Fecha de decisión2024-04-16

Código de productoGEX

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Co2 Laser System, Models: PureLase And VanLase is the device name listed in this FDA 510(k) record. The listed applicant is Cpmt Laser (Canadian Pioneer Medical Technology Corporation). It received FDA 510(k) clearance on 2024-04-16 under 510(k) number K232133. 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.

Preguntas frecuentes

What is the Co2 Laser System, Models: PureLase And VanLase?

Co2 Laser System, Models: PureLase And VanLase is a medical device that received FDA 510(k) clearance on 2024-04-16. The listed applicant is Cpmt Laser (Canadian Pioneer Medical Technology Corporation). The 510(k) number is K232133.

When did Co2 Laser System, Models: PureLase And VanLase receive FDA 510(k) clearance?

Co2 Laser System, Models: PureLase And VanLase received FDA 510(k) clearance on 2024-04-16, under 510(k) number K232133.

Who is the listed applicant for Co2 Laser System, Models: PureLase And VanLase?

The FDA 510(k) record lists Cpmt Laser (Canadian Pioneer Medical Technology Corporation) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Co2 Laser System, Models: PureLase And VanLase?

The FDA product code for Co2 Laser System, Models: PureLase And VanLase is GEX. This falls under the Gastroenterology category.

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Fuente oficial

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