EPIQ Series Diagnostic Ultrasound System

EPIQ Series Diagnostic Ultrasound System is an FDA 510(k)-cleared medical device (K233545) manufactured by Philips Ultrasound, LLC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 29, 2023. Regulation: 8.