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FDA 510(k)

LASER GAS MIXTURE

K-Number: K951045 · 1995-03-31

ApplicantLiquid Carbonic Industrial Gases
Decision Date1995-03-31
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LASER GAS MIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Liquid Carbonic Industrial Gases. It received FDA 510(k) clearance on 1995-03-31 under 510(k) number K951045. 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 LASER GAS MIXTURE?

LASER GAS MIXTURE is a medical device that received FDA 510(k) clearance on 1995-03-31. The listed applicant is Liquid Carbonic Industrial Gases. The 510(k) number is K951045.

When did LASER GAS MIXTURE receive FDA 510(k) clearance?

LASER GAS MIXTURE received FDA 510(k) clearance on 1995-03-31, under 510(k) number K951045.

Who is the listed applicant for LASER GAS MIXTURE?

The FDA 510(k) record lists Liquid Carbonic Industrial Gases as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASER GAS MIXTURE?

The FDA product code for LASER GAS MIXTURE is GEX. This falls under the Gastroenterology category.

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Official Source

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

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