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FDA 510(k)

ATHOS LASER

K-Number: K020072 · 2002-04-09

ApplicantQuantel Medical
Decision Date2002-04-09
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ATHOS LASER is the device name listed in this FDA 510(k) record. The listed applicant is Quantel Medical. It received FDA 510(k) clearance on 2002-04-09 under 510(k) number K020072. 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 ATHOS LASER?

ATHOS LASER is a medical device that received FDA 510(k) clearance on 2002-04-09. The listed applicant is Quantel Medical. The 510(k) number is K020072.

When did ATHOS LASER receive FDA 510(k) clearance?

ATHOS LASER received FDA 510(k) clearance on 2002-04-09, under 510(k) number K020072.

Who is the listed applicant for ATHOS LASER?

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

What is the FDA product code for ATHOS LASER?

The FDA product code for ATHOS LASER 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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