PCX-100 PATIENT INPUT LEADWIRE

PCX-100 PATIENT INPUT LEADWIRE is an FDA 510(k)-cleared medical device (K851632) manufactured by Eaton Medical Group. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 7, 1985. Regulation: 8.