FLEXIFLO OVER THE GUIDEWIRE JEJUNAL FEEDING TUBE— 510(k) K912972

Name: FDA 510(k) clearance K912972
Creator: U.S. Food and Drug Administration
Published: 1991-09-23

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K912972 for FLEXIFLO OVER THE GUIDEWIRE JEJUNAL FEEDING TUBE, Substantially Equivalent on 1991-09-23. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code FPD
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1991-07-08
Decision date: 1991-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, OH, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FPD

product code FPD

Death: 6
Other: 1
Total: 7

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.