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Philips Medical Systems
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DS ANTERIOR, DS BASE, DS HEAD-NECK, DS HEAD, FLEX (S,M,L) is an FDA 510(k)-cleared medical device (K123492) manufactured by Philips Medical Systems. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 12, 2012. Regulation: 8.