ACCUPUMP 901 (MODEL NUMBERS 50 & 100)

ACCUPUMP 901 (MODEL NUMBERS 50 & 100) is an FDA 510(k)-cleared medical device (K953382) manufactured by Pharmaceutical Infusion Technologies, 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 October 16, 1995. Regulation: 8.