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FDA 510(k)

Retrograde Coronary Sinus Perfusion Cannulae

K-Number: K253203 · 2026-02-19

ApplicantMedtronic, Inc.
Decision Date2026-02-19
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Retrograde Coronary Sinus Perfusion Cannulae is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2026-02-19 under 510(k) number K253203. 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 Retrograde Coronary Sinus Perfusion Cannulae?

Retrograde Coronary Sinus Perfusion Cannulae is a medical device that received FDA 510(k) clearance on 2026-02-19. The listed applicant is Medtronic, Inc.. The 510(k) number is K253203.

When did Retrograde Coronary Sinus Perfusion Cannulae receive FDA 510(k) clearance?

Retrograde Coronary Sinus Perfusion Cannulae received FDA 510(k) clearance on 2026-02-19, under 510(k) number K253203.

Who is the listed applicant for Retrograde Coronary Sinus Perfusion Cannulae?

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

What is the FDA product code for Retrograde Coronary Sinus Perfusion Cannulae?

The FDA product code for Retrograde Coronary Sinus Perfusion Cannulae 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 ReactorsK253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, Inc.K253106AngioVac CannulaAngioDynamics, 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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