
Lasag AG
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LASAG MICRORUPTER 2 ND:YAG LASER TRABECULOPLASTY is an FDA 510(k)-cleared medical device (K900199) manufactured by Lasag AG. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 26, 1990. Regulation: 8.

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