FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE

FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE is an FDA 510(k)-cleared medical device (K800406) manufactured by A.D.T. Lab Industries. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 11, 1980. Regulation: 8.