ENTERA-FLO FEEDING TUBE
K-Number: K901130 · 1990-06-01
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Device Summary
Frequently Asked Questions
What is the ENTERA-FLO FEEDING TUBE?
ENTERA-FLO FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1990-06-01. The listed applicant is Fresenius Pharma. The 510(k) number is K901130.
When did ENTERA-FLO FEEDING TUBE receive FDA 510(k) clearance?
ENTERA-FLO FEEDING TUBE received FDA 510(k) clearance on 1990-06-01, under 510(k) number K901130.
Who is the listed applicant for ENTERA-FLO FEEDING TUBE?
The FDA 510(k) record lists Fresenius Pharma as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENTERA-FLO FEEDING TUBE?
The FDA product code for ENTERA-FLO FEEDING 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 Fresenius Pharma 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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