CANNULAS, DYNACOR'S NASAL OXYGEN
K-Number: K790056 · 1979-02-05
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Device Summary
Frequently Asked Questions
What is the CANNULAS, DYNACOR'S NASAL OXYGEN?
CANNULAS, DYNACOR'S NASAL OXYGEN is a medical device that received FDA 510(k) clearance on 1979-02-05. The listed applicant is Medline Industries, Inc.. The 510(k) number is K790056.
When did CANNULAS, DYNACOR'S NASAL OXYGEN receive FDA 510(k) clearance?
CANNULAS, DYNACOR'S NASAL OXYGEN received FDA 510(k) clearance on 1979-02-05, under 510(k) number K790056.
Who is the listed applicant for CANNULAS, DYNACOR'S NASAL OXYGEN?
The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CANNULAS, DYNACOR'S NASAL OXYGEN?
The FDA product code for CANNULAS, DYNACOR'S NASAL OXYGEN 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 Medline Industries, 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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