Light Age, Inc.
EPICARE-DUO LASER SYSTEM
SKU K091625UPC GEX
In Stock
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IIFDA 510(k) Cleared (K091625)
1
Free shipping on orders over $99 · 30-day returns
Light Age, Inc.
Free shipping on orders over $99 · 30-day returns
EPICARE-DUO LASER SYSTEM is an FDA 510(k)-cleared medical device (K091625) manufactured by Light Age, Inc.. 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 November 2, 2009. Regulation: 8.
