AIR ENRICHER
K-Number: K761213 · 1976-12-16
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Device Summary
Frequently Asked Questions
What is the AIR ENRICHER?
AIR ENRICHER is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Union Carbide Corp.. The 510(k) number is K761213.
When did AIR ENRICHER receive FDA 510(k) clearance?
AIR ENRICHER received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761213.
Who is the listed applicant for AIR ENRICHER?
The FDA 510(k) record lists Union Carbide Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIR ENRICHER?
The FDA product code for AIR ENRICHER is CAW.
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 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: CAW)
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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