CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING

CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING is an FDA 510(k)-cleared medical device (K953750) manufactured by Boston Scientific Corp. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 10, 1996. Regulation: 8.