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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 a medical device manufactured by Medtronic, Inc.. It received FDA 510(k) clearance on 2026-02-19 under approval 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. It is manufactured by Medtronic, Inc.. The 510(k) number is K253203.

When was Retrograde Coronary Sinus Perfusion Cannulae approved by the FDA?

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

What company makes Retrograde Coronary Sinus Perfusion Cannulae?

Retrograde Coronary Sinus Perfusion Cannulae is manufactured by Medtronic, Inc..

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

The FDA product code for Retrograde Coronary Sinus Perfusion Cannulae is DWF.

Related Clinical Trials

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Related Devices (Code: 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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