IMPULSE 4000 DEFIBRILLATOR/TRANSCUTANEOUS PACER ANALYZER

IMPULSE 4000 DEFIBRILLATOR/TRANSCUTANEOUS PACER ANALYZER is an FDA 510(k)-cleared medical device (K941404) manufactured by Hogan & Hartson. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 28, 1994. Regulation: 8.