BLOOD GAS MIXTURE
K-Number: K822753 · 1982-10-22
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Device Summary
Frequently Asked Questions
What is the BLOOD GAS MIXTURE?
BLOOD GAS MIXTURE is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is Liquid Carbonic Corp.. The 510(k) number is K822753.
When did BLOOD GAS MIXTURE receive FDA 510(k) clearance?
BLOOD GAS MIXTURE received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822753.
Who is the listed applicant for BLOOD GAS MIXTURE?
The FDA 510(k) record lists Liquid Carbonic Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD GAS MIXTURE?
The FDA product code for 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.
Other records listing Liquid Carbonic 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: 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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