MEDLINE PNEUMOPERITONEUM NEEDLE

MEDLINE PNEUMOPERITONEUM NEEDLE is an FDA 510(k)-cleared medical device (K111955) manufactured by Medline Industries, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 15, 2011. Regulation: 8.