MODEL 9200 VIS-U-SCAN

MODEL 9200 VIS-U-SCAN is an FDA 510(k)-cleared medical device (K801832) manufactured by Del Mar Avionics. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 26, 1980. Regulation: 8.