Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES

K-Number: K882209 · 1988-08-02

Decision Date1988-08-02
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES is the device name listed in this FDA 510(k) record. The listed applicant is Linde Div. Union Carbide Corp.. It received FDA 510(k) clearance on 1988-08-02 under 510(k) number K882209. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

↑