FDA awards 510(k) clearance to ProxiDiagnost N90 digital radiography-fluoroscopy system.- Royal Philips.
Royal Philips announced it has received 510(k) clearance from the FDA to market ProxiDiagnost N90, its latest Digital Radiography-Fluoroscopy (DRF) system. This digital radiography-fluoroscopy system supports high room utilization and throughput, accessible design and dose management features to benefit patients and staff.
The key advantage is its ability to perform both nearby fluoroscopy and digital X-rays through a single system. Meanwhile its Grid-Controlled Fluoroscopy system enables a dose rate reduction up to 68% compared to Pulse Controlled Fluoroscopy, depending on patient type and clinical application.
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