
Surgistar, Inc.
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SURGISTAR MICROKERATOME BLADE, MODEL NO. 2400-LSK is an FDA 510(k)-cleared medical device (K030891) manufactured by Surgistar, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 16, 2003. Regulation: 8.