InfiMed nets 510(k) clearance for DRF system

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InfiMed has received the FDA’s 510(k) approval for its Nexus-DRF multi-purpose digital imaging system, a new i 5 series product that combines radiofrequency (RF), digital radiography (DR) and cardiac capabilities on one imaging platform using various flat-panel detectors.

The Nexus-DRF is offered as either a full system technology or a software development kit, according to the Liverpool, N.Y.-based company.