NKA MODEL SEC-3102 CARDIAC STIMULATOR

NKA MODEL SEC-3102 CARDIAC STIMULATOR is an FDA 510(k)-cleared medical device (K894492) manufactured by Nihon Kohden America, 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 December 19, 1989. Regulation: 8.