BIODYNAMICS FEMORAL CANAL BRUSH #1201

BIODYNAMICS FEMORAL CANAL BRUSH #1201 is an FDA 510(k)-cleared medical device (K870349) manufactured by Biodynamic Technologies, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 12, 1987. Regulation: 8.