MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON)

MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON) is an FDA 510(k)-cleared medical device (K954284) manufactured by Medi-Plast Intl., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 11, 1996. Regulation: 8.