REGISTREX 1000 DIGITAL RADIOGRAPHY SYS

REGISTREX 1000 DIGITAL RADIOGRAPHY SYS is an FDA 510(k)-cleared medical device (K833230) manufactured by Advanced Technology Laboratories, 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 November 20, 1983. Regulation: 8.