SIEMENS ORTHOPHOS DS/DS CEPH

SIEMENS ORTHOPHOS DS/DS CEPH is an FDA 510(k)-cleared medical device (K972312) manufactured by Siemens AG. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 14, 1997. Regulation: 8.