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FDA 510(k)

CLINICAL BLOOD GAS MIXTURES

K-Number: K904163 · 1990-11-01

ApplicantNorco, Inc.
Decision Date1990-11-01
Product CodeLCH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLINICAL BLOOD GAS MIXTURES is the device name listed in this FDA 510(k) record. The listed applicant is Norco, Inc.. It received FDA 510(k) clearance on 1990-11-01 under 510(k) number K904163. The device is classified under product code LCH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINICAL BLOOD GAS MIXTURES?

CLINICAL BLOOD GAS MIXTURES is a medical device that received FDA 510(k) clearance on 1990-11-01. The listed applicant is Norco, Inc.. The 510(k) number is K904163.

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

CLINICAL BLOOD GAS MIXTURES received FDA 510(k) clearance on 1990-11-01, under 510(k) number K904163.

Who is the listed applicant for CLINICAL BLOOD GAS MIXTURES?

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

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

The FDA product code for CLINICAL BLOOD GAS MIXTURES is LCH.

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 Norco, Inc. 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: LCH)

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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