THE KEOFEED STOMACH TUBE
K-Number: K812507 · 1981-09-14
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Device Summary
Frequently Asked Questions
What is the THE KEOFEED STOMACH TUBE?
THE KEOFEED STOMACH TUBE is a medical device that received FDA 510(k) clearance on 1981-09-14. The listed applicant is Hedeco. The 510(k) number is K812507.
When did THE KEOFEED STOMACH TUBE receive FDA 510(k) clearance?
THE KEOFEED STOMACH TUBE received FDA 510(k) clearance on 1981-09-14, under 510(k) number K812507.
Who is the listed applicant for THE KEOFEED STOMACH TUBE?
The FDA 510(k) record lists Hedeco as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE KEOFEED STOMACH TUBE?
The FDA product code for THE KEOFEED STOMACH TUBE is KNT.
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 Hedeco 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: KNT)
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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