MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES
K-Number: K882209 · 1988-08-02
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Device Summary
Frequently Asked Questions
What is the MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES?
MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Linde Div. Union Carbide Corp.. The 510(k) number is K882209.
When did MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES receive FDA 510(k) clearance?
MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES received FDA 510(k) clearance on 1988-08-02, under 510(k) number K882209.
Who is the listed applicant for MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES?
The FDA 510(k) record lists Linde Div. Union Carbide Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES?
The FDA product code for MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES is CHL.
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 Linde Div. Union Carbide Corp. 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: CHL)
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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