K-number	K250325
Device name	BD Alaris Pump Infusion Set
Applicant	Carefusion (Bd)
Product code	FPA
Device class	Class II
Decision date	Oct 30, 2025
Decision	Substantially Equivalent
Regulation	880.5440

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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BD Alaris Pump Infusion Set

Everything you need for a 510(k) submission. Nothing you don't.