TEMPORARY SCREENING LEAD/CATHETER KIT

TEMPORARY SCREENING LEAD/CATHETER KIT is an FDA 510(k)-cleared medical device (K934938) manufactured by Medtronic Vascular. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 13, 1994. Regulation: 8.