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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 the device name listed in this FDA 510(k) record. The listed applicant is AngioDynamics, Inc.. It received FDA 510(k) clearance on 2025-10-24 under 510(k) 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. The listed applicant is AngioDynamics, Inc.. The 510(k) number is K253106.

When did AngioVac Cannula receive FDA 510(k) clearance?

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

Who is the listed applicant for AngioVac Cannula?

The FDA 510(k) record lists AngioDynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AngioVac Cannula?

The FDA product code for AngioVac Cannula is DWF.

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Related Devices (Code: DWF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, Inc.

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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