EPIQ Series Diagnostic Ultrasound Systems

EPIQ Series Diagnostic Ultrasound Systems is an FDA 510(k)-cleared medical device (K202216) manufactured by Philips Ultrasound, 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 September 1, 2020. Regulation: 8.