AVALON GENERAL PURPOSE SCANNER, PREVIEW GP

AVALON GENERAL PURPOSE SCANNER, PREVIEW GP is an FDA 510(k)-cleared medical device (K904317) manufactured by Avalon Technology Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 12, 1991. Regulation: 8.