CLINICAL BLOOD GAS MIXTURES
K-Number: K904163 · 1990-11-01
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Device Summary
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
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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