SPRING-WOUND EPIDURAL CATHETER

SPRING-WOUND EPIDURAL CATHETER is an FDA 510(k)-cleared medical device (K991879) manufactured by Micor, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 27, 1999. Regulation: 8.