CARDIMA SEEKER AND STUBBIE GUIDEWIRES

CARDIMA SEEKER AND STUBBIE GUIDEWIRES is an FDA 510(k)-cleared medical device (K932801) manufactured by Cardima, 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 August 31, 1993. Regulation: 8.