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Medtronic Xomed
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MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE is an FDA 510(k)-cleared medical device (K000728) manufactured by Medtronic Xomed. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 20, 2000. Regulation: 8.