G.E. DXD 325/350/350II/DXD 525/525II GENERATORS

G.E. DXD 325/350/350II/DXD 525/525II GENERATORS is an FDA 510(k)-cleared medical device (K902986) manufactured by Electromek Diagnostic Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 12, 1991. Regulation: 8.