CORE BIOPSY NEEDLE, CATALOG CODE #54006

CORE BIOPSY NEEDLE, CATALOG CODE #54006 is an FDA 510(k)-cleared medical device (K891537) manufactured by Dlp, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 17, 1989. Regulation: 8.