BAKER INTESTINAL TUBE, TWIN CUFF
K-Number: K792333 · 1980-01-16
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Device Summary
Frequently Asked Questions
What is the BAKER INTESTINAL TUBE, TWIN CUFF?
BAKER INTESTINAL TUBE, TWIN CUFF is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is Intl. Hospital Products, Inc.. The 510(k) number is K792333.
When did BAKER INTESTINAL TUBE, TWIN CUFF receive FDA 510(k) clearance?
BAKER INTESTINAL TUBE, TWIN CUFF received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792333.
Who is the listed applicant for BAKER INTESTINAL TUBE, TWIN CUFF?
The FDA 510(k) record lists Intl. Hospital Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BAKER INTESTINAL TUBE, TWIN CUFF?
The FDA product code for BAKER INTESTINAL TUBE, TWIN CUFF 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 Intl. Hospital Products, 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: 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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