NASAL, OXYGEN, CANNULA
K-Number: K790885 · 1979-05-17
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Device Summary
Frequently Asked Questions
What is the NASAL, OXYGEN, CANNULA?
NASAL, OXYGEN, CANNULA is a medical device that received FDA 510(k) clearance on 1979-05-17. The listed applicant is Airlife, Inc.. The 510(k) number is K790885.
When did NASAL, OXYGEN, CANNULA receive FDA 510(k) clearance?
NASAL, OXYGEN, CANNULA received FDA 510(k) clearance on 1979-05-17, under 510(k) number K790885.
Who is the listed applicant for NASAL, OXYGEN, CANNULA?
The FDA 510(k) record lists Airlife, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NASAL, OXYGEN, CANNULA?
The FDA product code for NASAL, OXYGEN, CANNULA is CAT.
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 Airlife, 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: CAT)
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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