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FDA 510(k)

LUNG DIFFUSION GAS MIXTURE

K-Number: K924796 · 1992-12-17

Decision Date1992-12-17
Product CodeBXK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LUNG DIFFUSION GAS MIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Gulf States Airgas. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K924796. The device is classified under product code BXK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNG DIFFUSION GAS MIXTURE?

LUNG DIFFUSION GAS MIXTURE is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Gulf States Airgas. The 510(k) number is K924796.

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

LUNG DIFFUSION GAS MIXTURE received FDA 510(k) clearance on 1992-12-17, under 510(k) number K924796.

Who is the listed applicant for LUNG DIFFUSION GAS MIXTURE?

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

What is the FDA product code for LUNG DIFFUSION GAS MIXTURE?

The FDA product code for LUNG DIFFUSION GAS MIXTURE is BXK.

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 Gulf States Airgas 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: BXK)

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

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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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