Buckman Co., Inc.
FUTURELASE 3000/3002 ERBIUM LASER SYSTEM
SKU K974641UPC GEX
In Stock
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IIFDA 510(k) Cleared (K974641)
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Free shipping on orders over $99 · 30-day returns
Buckman Co., Inc.
Free shipping on orders over $99 · 30-day returns
FUTURELASE 3000/3002 ERBIUM LASER SYSTEM is an FDA 510(k)-cleared medical device (K974641) manufactured by Buckman Co., 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 June 7, 1998. Regulation: 8.
