LASER GAS MIXTURE
K-Number: K942865 · 1994-08-23
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Device Summary
Frequently Asked Questions
What is the LASER GAS MIXTURE?
LASER GAS MIXTURE is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Nordan Smith Welding Supplies. The 510(k) number is K942865.
When did LASER GAS MIXTURE receive FDA 510(k) clearance?
LASER GAS MIXTURE received FDA 510(k) clearance on 1994-08-23, under 510(k) number K942865.
Who is the listed applicant for LASER GAS MIXTURE?
The FDA 510(k) record lists Nordan Smith Welding Supplies 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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Nordan Smith Welding Supplies as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GEX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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