CARNATION OXYGEN
K-Number: K850626 · 1985-03-12
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Device Summary
Frequently Asked Questions
What is the CARNATION OXYGEN?
CARNATION OXYGEN is a medical device that received FDA 510(k) clearance on 1985-03-12. The listed applicant is Cathay Consolidated, Inc.. The 510(k) number is K850626.
When did CARNATION OXYGEN receive FDA 510(k) clearance?
CARNATION OXYGEN received FDA 510(k) clearance on 1985-03-12, under 510(k) number K850626.
Who is the listed applicant for CARNATION OXYGEN?
The FDA 510(k) record lists Cathay Consolidated, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARNATION OXYGEN?
The FDA product code for CARNATION OXYGEN is BYG.
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 Cathay Consolidated, 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: BYG)
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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