510 CARBINETTE X-RAY UNIT

510 CARBINETTE X-RAY UNIT is an FDA 510(k)-cleared medical device (K790392) manufactured by General X-Ray, 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 March 25, 1979. Regulation: 8.