MTHF-9S MOBIL C-ARM IMAGE INTENSIFIER UNIT

MTHF-9S MOBIL C-ARM IMAGE INTENSIFIER UNIT is an FDA 510(k)-cleared medical device (K900194) manufactured by Imt America, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 6, 1990. Regulation: 8.