G.E. MSI 850/850II/1250 THREE PHASE GENERATORS

G.E. MSI 850/850II/1250 THREE PHASE GENERATORS is an FDA 510(k)-cleared medical device (K902988) 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.