BIOMID BONE MARROW BIOPSY NEEDLE

BIOMID BONE MARROW BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K962569) manufactured by Gallini Intl., Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 26, 1996. Regulation: 8.