CUSHMAN MANUFACTURING, INC. ULTRA 6.0.

CUSHMAN MANUFACTURING, INC. ULTRA 6.0. is an FDA 510(k)-cleared medical device (K960802) manufactured by Cushman Mfg., 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 June 17, 1996. Regulation: 8.