Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

QuickDraw Venous Cannula

K-Number: K200499 · 2020-03-29

ApplicantEdwards Lifesciences, LLC
Decision Date2020-03-29
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QuickDraw Venous Cannula is a medical device manufactured by Edwards Lifesciences, LLC. It received FDA 510(k) clearance on 2020-03-29 under approval number K200499. 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 QuickDraw Venous Cannula?

QuickDraw Venous Cannula is a medical device that received FDA 510(k) clearance on 2020-03-29. It is manufactured by Edwards Lifesciences, LLC. The 510(k) number is K200499.

When was QuickDraw Venous Cannula approved by the FDA?

QuickDraw Venous Cannula received FDA 510(k) clearance on 2020-03-29, under approval number K200499.

What company makes QuickDraw Venous Cannula?

QuickDraw Venous Cannula is manufactured by Edwards Lifesciences, LLC.

What is the FDA product code for QuickDraw Venous Cannula?

The FDA product code for QuickDraw Venous Cannula is DWF.

Related Clinical Trials

NCT07510451 The Hypotension Prediction Index Versus Standard Advanced Haemodynamic Monitoring in Patients Undergoing Major Aortic Surgery RECRUITING

Other Devices by Edwards Lifesciences, LLC

K161962VAMP Venous/Arterial Blood Management Protection System K160645PreSep Oligon Oximetry Catheter K160552EV1000 Clinical Platform with ClearSight Finger Cuff or ClearSight System, EV1000 Clinical Platform K160084Swan Ganz Catheters K152980Flo Trac sensor, Volume View sensor K172660Duravess bovine pericardial vascular patch

View all 64 devices →

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.

↑