GILLAM-TUKEL BONE MARROW BIOPSY NEEDLE

GILLAM-TUKEL BONE MARROW BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K924501) manufactured by Symbiosis Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 19, 1993. Regulation: 8.