THE MURRAY MOBILIFT(TM)

THE MURRAY MOBILIFT(TM) is an FDA 510(k)-cleared medical device (K895677) manufactured by Medical/Surgical Specialties, Ltd.. 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 25, 1990. Regulation: 8.