OXYGEN CANNULA
K-Number: K770996 · 1977-06-29
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Device Summary
Frequently Asked Questions
What is the OXYGEN CANNULA?
OXYGEN CANNULA is a medical device that received FDA 510(k) clearance on 1977-06-29. The listed applicant is Ohio Medical Products. The 510(k) number is K770996.
When did OXYGEN CANNULA receive FDA 510(k) clearance?
OXYGEN CANNULA received FDA 510(k) clearance on 1977-06-29, under 510(k) number K770996.
Who is the listed applicant for OXYGEN CANNULA?
The FDA 510(k) record lists Ohio Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYGEN CANNULA?
The FDA product code for 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 Ohio Medical Products 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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