TEMPORARY SCREENING LEAD/ CATHETER KIT

TEMPORARY SCREENING LEAD/ CATHETER KIT is an FDA 510(k)-cleared medical device (K934939) manufactured by Medtronic Vascular. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 23, 1995. Regulation: 8.