Philips Lumify Diagnostic Ultrasound System

Philips Lumify Diagnostic Ultrasound System is an FDA 510(k)-cleared medical device (K152899) manufactured by Philips Healthcare, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 29, 2015. Regulation: 8.