CANNULA, NASAL, FOR OXYGEN
K-Number: K760080 · 1976-07-15
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Device Summary
Frequently Asked Questions
What is the CANNULA, NASAL, FOR OXYGEN?
CANNULA, NASAL, FOR OXYGEN is a medical device that received FDA 510(k) clearance on 1976-07-15. The listed applicant is Inspiron Corp.. The 510(k) number is K760080.
When did CANNULA, NASAL, FOR OXYGEN receive FDA 510(k) clearance?
CANNULA, NASAL, FOR OXYGEN received FDA 510(k) clearance on 1976-07-15, under 510(k) number K760080.
Who is the listed applicant for CANNULA, NASAL, FOR OXYGEN?
The FDA 510(k) record lists Inspiron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CANNULA, NASAL, FOR OXYGEN?
The FDA product code for CANNULA, NASAL, FOR 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 Inspiron Corp. 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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