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FDA 510(k)

AngioVac Cannula

K-Number: K253106 · 2025-10-24

ApplicantAngioDynamics, Inc.
Decision Date2025-10-24
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AngioVac Cannula is a medical device manufactured by AngioDynamics, Inc.. It received FDA 510(k) clearance on 2025-10-24 under approval number K253106. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AngioVac Cannula?

AngioVac Cannula is a medical device that received FDA 510(k) clearance on 2025-10-24. It is manufactured by AngioDynamics, Inc.. The 510(k) number is K253106.

When was AngioVac Cannula approved by the FDA?

AngioVac Cannula received FDA 510(k) clearance on 2025-10-24, under approval number K253106.

What company makes AngioVac Cannula?

AngioVac Cannula is manufactured by AngioDynamics, Inc..

What is the FDA product code for AngioVac Cannula?

The FDA product code for AngioVac Cannula is DWF.

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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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