BD ULTRA-FINE III PEN NEEDLE— 510(k) K024109

Substantially Equivalent

Becton, Dickinson & CO

FDA 510(k) clearance K024109 for BD ULTRA-FINE III PEN NEEDLE, Substantially Equivalent on 2002-12-30. Applicant: Becton, Dickinson & CO.

Clearance details

Applicant: Becton, Dickinson & CO
Product code: Code FMI
Advisory panel: General Hospital
Date received: 2002-12-13
Decision date: 2002-12-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Franklin Lakes, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMI

product code FMI

Death: 28
Injury: 1,517
Malfunction: 23,981
Other: 18
Total: 25,544

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.