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FDA 510(k)

MEDICAL LASER MIXTURE

K-Number: K935310 · 1993-12-23

ApplicantAcetylene Gas Co.
Decision Date1993-12-23
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDICAL LASER MIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Acetylene Gas Co.. It received FDA 510(k) clearance on 1993-12-23 under 510(k) number K935310. 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 MEDICAL LASER MIXTURE?

MEDICAL LASER MIXTURE is a medical device that received FDA 510(k) clearance on 1993-12-23. The listed applicant is Acetylene Gas Co.. The 510(k) number is K935310.

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

MEDICAL LASER MIXTURE received FDA 510(k) clearance on 1993-12-23, under 510(k) number K935310.

Who is the listed applicant for MEDICAL LASER MIXTURE?

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

What is the FDA product code for MEDICAL LASER MIXTURE?

The FDA product code for MEDICAL LASER 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.

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Other records listing Acetylene Gas Co. 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.

K935309LUNG DIFFUSIONK935311CLINICAL BLOOD GAS

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.

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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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