FDA clears Boston Scis Renegade HI-FLO for embolisms

The FDA has approved Boston Scientific’s Renegade HI-FLO Fathom system for selective access and delivery of diagnostic, embolic and therapeutic materials to the peripheral vasculature.

According to company, the Renegade HI-FLO is intended for use by interventional radiologists to treat uterine fibroids and liver cancer. Natick, Mass.-based Boston Scientific said that the system combines turn-for-turn torque response with the Fathom-16 and the Renegade HI-FLO Microcatheter pre-loaded as a single platform, which will be adaptable to a range of embolization procedures via eight configurations.

Around the web

The new guidelines were designed to ensure sonographers and other members of the heart team have the information they need to screen patients when appropriate and identify early warnings signs of PH. 

Harvard’s David A. Rosman, MD, MBA, explains how moving imaging outside of hospitals could save billions of dollars for U.S. healthcare.

Back in September, the FDA approved GE HealthCare’s new PET radiotracer, flurpiridaz F-18, for patients with known or suspected CAD. It is seen by many in the industry as a major step forward in patient care.