AIR BED & FLOTATION DERMAGARD 800 & 900 SYSTEMS

AIR BED & FLOTATION DERMAGARD 800 & 900 SYSTEMS is an FDA 510(k)-cleared medical device (K882229) manufactured by Biologics Intl., Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 15, 1988. Regulation: 8.