STRYKER ANTIMIC CATHETER

STRYKER ANTIMIC CATHETER is an FDA 510(k)-cleared medical device (K072702) manufactured by Stryker Instruments, Instruments Div.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 2008. Regulation: 8.