The Netherlands-based Royal Philips has obtained 510(k) approval from the US Food and Drug Administration (FDA) for the spectral breast density measurement application for use with its MicroDose SI full-field digital mammography (FFDM) ...
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Royal Philips Electronics' full-field digital mammography (FFDM) system. Having the capability to enable future Single-Shot Spectral Imaging applications like ...
Tags: FDA, clinicians, FFDM