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FDA 510(k)

DLP Silicone Coronary Artery Ostial Cannulae

K-Number: K231206 · 2023-12-07

ApplicantMedtronic, Inc.
Decision Date2023-12-07
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DLP Silicone Coronary Artery Ostial Cannulae is a medical device manufactured by Medtronic, Inc.. It received FDA 510(k) clearance on 2023-12-07 under approval number K231206. 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 DLP Silicone Coronary Artery Ostial Cannulae?

DLP Silicone Coronary Artery Ostial Cannulae is a medical device that received FDA 510(k) clearance on 2023-12-07. It is manufactured by Medtronic, Inc.. The 510(k) number is K231206.

When was DLP Silicone Coronary Artery Ostial Cannulae approved by the FDA?

DLP Silicone Coronary Artery Ostial Cannulae received FDA 510(k) clearance on 2023-12-07, under approval number K231206.

What company makes DLP Silicone Coronary Artery Ostial Cannulae?

DLP Silicone Coronary Artery Ostial Cannulae is manufactured by Medtronic, Inc..

What is the FDA product code for DLP Silicone Coronary Artery Ostial Cannulae?

The FDA product code for DLP Silicone Coronary Artery Ostial Cannulae is DWF.

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Related Devices (Code: DWF)

K162214Protek Solo 24 Fr Venous Cannula SetCardiacassist, Inc. K160257PROTEK Duo 31 Fr. Veno-Venous Cannula SetCardiacassist, Inc. K153598Medtronic Bio-Medicus Adult Cannula KitMedtronic, Inc. K171979Tubing PackMedtronic, Inc. K170488Peak Left Ventricular Vent Cannula, 20 Fr.; Peak Left Ventricular Vent Cannula, 18 Fr; Peak Left Ventricular Vent Cannula, 16 FrSurge Cardiovascular K162215Aortic Arch Cannulae, Optiflow Aortic Arch CannulaeSorin Group Italia S.R.L.

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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