
3D Line USA, Inc.
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DYNATRAC, COD. 50-1A is an FDA 510(k)-cleared medical device (K034051) manufactured by 3D Line USA, 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 April 4, 2004. Regulation: 8.