Cutera, Inc.
CUTERA GENESISPLUS LASER SYSTEM
SKU K103626UPC PDZ
In Stock
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IIFDA 510(k) Cleared (K103626)
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Free shipping on orders over $99 · 30-day returns
Cutera, Inc.
Free shipping on orders over $99 · 30-day returns
CUTERA GENESISPLUS LASER SYSTEM is an FDA 510(k)-cleared medical device (K103626) manufactured by Cutera, 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 April 4, 2011. Regulation: 8.
