FLEXIFLO 60 NASOJEJUNAL FEEDING TUBE
K-Number: K924996 · 1993-10-08
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Device Summary
Frequently Asked Questions
What is the FLEXIFLO 60 NASOJEJUNAL FEEDING TUBE?
FLEXIFLO 60 NASOJEJUNAL FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is Abbott Laboratories. The 510(k) number is K924996.
When did FLEXIFLO 60 NASOJEJUNAL FEEDING TUBE receive FDA 510(k) clearance?
FLEXIFLO 60 NASOJEJUNAL FEEDING TUBE received FDA 510(k) clearance on 1993-10-08, under 510(k) number K924996.
Who is the listed applicant for FLEXIFLO 60 NASOJEJUNAL 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 60 NASOJEJUNAL FEEDING TUBE?
The FDA product code for FLEXIFLO 60 NASOJEJUNAL 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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