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Lapis Lazuli International NV
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EYE SEE MULTIPURPOSE CONTACT LENS SOLUTION is an FDA 510(k)-cleared medical device (K070767) manufactured by Lapis Lazuli International NV. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 23, 2007. Regulation: 8.