DYNASTY GC 12400 (GELL/CELL)

DYNASTY GC 12400 (GELL/CELL) is an FDA 510(k)-cleared medical device (K942308) manufactured by Foley & Lardner. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 6, 1994. Regulation: 8.