GASTROINTESTINAL TUBES AND ACCESSORIES
K-Number: K901023 · 1990-07-02
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Device Summary
Frequently Asked Questions
What is the GASTROINTESTINAL TUBES AND ACCESSORIES?
GASTROINTESTINAL TUBES AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1990-07-02. The listed applicant is Medline Industries, Inc.. The 510(k) number is K901023.
When did GASTROINTESTINAL TUBES AND ACCESSORIES receive FDA 510(k) clearance?
GASTROINTESTINAL TUBES AND ACCESSORIES received FDA 510(k) clearance on 1990-07-02, under 510(k) number K901023.
Who is the listed applicant for GASTROINTESTINAL TUBES AND ACCESSORIES?
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 GASTROINTESTINAL TUBES AND ACCESSORIES?
The FDA product code for GASTROINTESTINAL TUBES AND ACCESSORIES 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 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: 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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