FLEXIFLO NASOENTERIC FEEDING TUBE
K-Number: K922217 · 1995-03-01
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Device Summary
Frequently Asked Questions
What is the FLEXIFLO NASOENTERIC FEEDING TUBE?
FLEXIFLO NASOENTERIC FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is Abbott Laboratories. The 510(k) number is K922217.
When did FLEXIFLO NASOENTERIC FEEDING TUBE receive FDA 510(k) clearance?
FLEXIFLO NASOENTERIC FEEDING TUBE received FDA 510(k) clearance on 1995-03-01, under 510(k) number K922217.
Who is the listed applicant for FLEXIFLO NASOENTERIC FEEDING TUBE?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIFLO NASOENTERIC FEEDING TUBE?
The FDA product code for FLEXIFLO NASOENTERIC 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 Abbott Laboratories 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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