Radical Catheter Technologies has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its 6F neurovascular access catheter.
6F is the company's third FDA-cleared catheter and is designed to broaden therapeutic options for middle-meningeal artery embolization and radial access procedures, according to the firm. It is built on patented ribbon technology intended to provide simultaneous flexibility, push, and stability, with a thinner wall construction that offers a greater inner diameter relative to outer diameter, Radical Catheter Technologies said.
![A 53-year-old patient (patient number four) with a recurrent pituitary adenoma with extension of a cystic component of disease to the medial temporal lobe apparent on MRI (contoured in blue), and extension of disease to the left sphenoid bone and orbital apex apparent on [68Ga]Ga-DOTA-TATE (contoured in yellow).](https://img.auntminnie.com/mindful/smg/workspaces/default/uploads/2026/04/pituitary-tumor.QGsEnyB4bU.jpg?auto=format%2Ccompress&fit=crop&h=100&q=70&w=100)
![A 53-year-old patient (patient number four) with a recurrent pituitary adenoma with extension of a cystic component of disease to the medial temporal lobe apparent on MRI (contoured in blue), and extension of disease to the left sphenoid bone and orbital apex apparent on [68Ga]Ga-DOTA-TATE (contoured in yellow).](https://img.auntminnie.com/mindful/smg/workspaces/default/uploads/2026/04/pituitary-tumor.QGsEnyB4bU.jpg?auto=format%2Ccompress&dpr=2&fit=crop&h=167&q=70&w=250)
