G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN

G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN is an FDA 510(k)-cleared medical device (K902985) 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 18, 1990. Regulation: 8.