PLETHYSMOGRAPH (MDI SYSTEM II)

PLETHYSMOGRAPH (MDI SYSTEM II) is an FDA 510(k)-cleared medical device (K760504) manufactured by Marketing Development Intl.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 25, 1976. Regulation: 8.