G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS

G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS is an FDA 510(k)-cleared medical device (K902987) 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 December 25, 1990. Regulation: 8.