CARROM CARELIFE SERIES 40000 MODULAR BES SYSTEM

CARROM CARELIFE SERIES 40000 MODULAR BES SYSTEM is an FDA 510(k)-cleared medical device (K854937) manufactured by Carrom Healthcare, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 3, 1986. Regulation: 8.