INTER-PAL C-19 AND INTER-PAL C-38

INTER-PAL C-19 AND INTER-PAL C-38 is an FDA 510(k)-cleared medical device (K890294) manufactured by Enrad Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 31, 1990. Regulation: 8.