OMNIMED NASAL OXYGEN CANNULA
K-Number: K850066 · 1985-01-24
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Device Summary
Frequently Asked Questions
What is the OMNIMED NASAL OXYGEN CANNULA?
OMNIMED NASAL OXYGEN CANNULA is a medical device that received FDA 510(k) clearance on 1985-01-24. The listed applicant is Omni Intl., Inc.. The 510(k) number is K850066.
When did OMNIMED NASAL OXYGEN CANNULA receive FDA 510(k) clearance?
OMNIMED NASAL OXYGEN CANNULA received FDA 510(k) clearance on 1985-01-24, under 510(k) number K850066.
Who is the listed applicant for OMNIMED NASAL OXYGEN CANNULA?
The FDA 510(k) record lists Omni Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OMNIMED NASAL OXYGEN CANNULA?
The FDA product code for OMNIMED 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 Omni Intl., 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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