K-number	K253106
Device name	AngioVac Cannula
Applicant	AngioDynamics, Inc.
Product code	DWF
Device class	Class II
Decision date	Oct 24, 2025
Decision	Substantially Equivalent
Regulation	870.4210

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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AngioVac Cannula

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