STRATO PLAST PORT INTRO KT(10 FR)LPS 7013/MODIFIED

STRATO PLAST PORT INTRO KT(10 FR)LPS 7013/MODIFIED is an FDA 510(k)-cleared medical device (K905852) manufactured by Strato Medical Corp.. 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 April 18, 1991. Regulation: 8.