
Laser Surgical Systems
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KTP/532, KTP/YAG AND KTP/YAG XP is an FDA 510(k)-cleared medical device (K931445) manufactured by Laser Surgical Systems. 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 December 1, 1994. Regulation: 8.