SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE

SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE is an FDA 510(k)-cleared medical device (K890926) manufactured by Meadox Surgimed, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 19, 1989. Regulation: 8.