Siemens 3.0T PROCURE Array Coil

Siemens 3.0T PROCURE Array Coil is an FDA 510(k)-cleared medical device (K142676) manufactured by Resonance Innovations, 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 December 4, 2014. Regulation: 8.