GASTROINTESTINAL TUBE AND ACCESSORIES
K-Number: K914492 · 1992-02-25
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Device Summary
Frequently Asked Questions
What is the GASTROINTESTINAL TUBE AND ACCESSORIES?
GASTROINTESTINAL TUBE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1992-02-25. The listed applicant is Sandoz Nutrition. The 510(k) number is K914492.
When did GASTROINTESTINAL TUBE AND ACCESSORIES receive FDA 510(k) clearance?
GASTROINTESTINAL TUBE AND ACCESSORIES received FDA 510(k) clearance on 1992-02-25, under 510(k) number K914492.
Who is the listed applicant for GASTROINTESTINAL TUBE AND ACCESSORIES?
The FDA 510(k) record lists Sandoz Nutrition as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GASTROINTESTINAL TUBE AND ACCESSORIES?
The FDA product code for GASTROINTESTINAL TUBE AND ACCESSORIES is FPD.
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 Sandoz Nutrition 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: FPD)
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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