STRATO PORT INTRODUCER KT(10 FR) LPS 5013/MODIFIED

STRATO PORT INTRODUCER KT(10 FR) LPS 5013/MODIFIED is an FDA 510(k)-cleared medical device (K905839) 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.