ZOLL D 5400 ADULT SOLID GEL DEFIBRILLATION ELECTRO

ZOLL D 5400 ADULT SOLID GEL DEFIBRILLATION ELECTRO is an FDA 510(k)-cleared medical device (K931804) manufactured by Zoll Medical 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 October 7, 1993. Regulation: 8.