The U.S. Food and Drug Administration (FDA) has granted InfiMed 510(k) market clearance for its i5 Nexus-DRF multi-purpose digital imaging system. The new i5 product line combines radiographic fluoroscopy (RF), digital radiography (DR) and cardiac capabilities on one imaging platform using various industry-leading flat panel detectors.
The Nexus-DRF is offered as either a full system solution, or a software development kit (SDK). Coupled with its multi-modality and multi-detector flexibility, the high-performance technology built into the Nexus-DRF makes this system a true value add for any original equipment manufacturer (OEM) imaging product portfolio.
For more information: www.infimed.com