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FDA 510(k)

YOULASER CO2 LASER SYSTEM

K-Number: K111592 · 2011-08-25

ApplicantQuanta System Spa
Decision Date2011-08-25
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YOULASER CO2 LASER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Quanta System Spa. It received FDA 510(k) clearance on 2011-08-25 under 510(k) number K111592. 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.

Frequently Asked Questions

What is the YOULASER CO2 LASER SYSTEM?

YOULASER CO2 LASER SYSTEM is a medical device that received FDA 510(k) clearance on 2011-08-25. The listed applicant is Quanta System Spa. The 510(k) number is K111592.

When did YOULASER CO2 LASER SYSTEM receive FDA 510(k) clearance?

YOULASER CO2 LASER SYSTEM received FDA 510(k) clearance on 2011-08-25, under 510(k) number K111592.

Who is the listed applicant for YOULASER CO2 LASER SYSTEM?

The FDA 510(k) record lists Quanta System Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YOULASER CO2 LASER SYSTEM?

The FDA product code for YOULASER CO2 LASER SYSTEM is GEX. This falls under the Gastroenterology category.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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