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FDA 510(k)

CLINICAL BLOOD GAS MIXTURE

K-Number: K944812 · 1995-02-01

Decision Date1995-02-01
Product CodeBXK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CLINICAL BLOOD GAS MIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Laboratory & Specialty Gases, Inc.. It received FDA 510(k) clearance on 1995-02-01 under 510(k) number K944812. 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 CLINICAL BLOOD GAS MIXTURE?

CLINICAL BLOOD GAS MIXTURE is a medical device that received FDA 510(k) clearance on 1995-02-01. The listed applicant is Laboratory & Specialty Gases, Inc.. The 510(k) number is K944812.

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

CLINICAL BLOOD GAS MIXTURE received FDA 510(k) clearance on 1995-02-01, under 510(k) number K944812.

Who is the listed applicant for CLINICAL BLOOD GAS MIXTURE?

The FDA 510(k) record lists Laboratory & Specialty Gases, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLINICAL BLOOD GAS MIXTURE?

The FDA product code for CLINICAL BLOOD 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.

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

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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