UNIPORT MODELS SD-90, TD-60, TD-70 & TD-90

UNIPORT MODELS SD-90, TD-60, TD-70 & TD-90 is an FDA 510(k)-cleared medical device (K873575) manufactured by Healthcare 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 November 12, 1987. Regulation: 8.