Sandstone Medical Technologies, LLC
CHEVEUX DIODE LASER SYSTEM
SKU K100893UPC GEX
In Stock
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IIFDA 510(k) Cleared (K100893)
1
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Sandstone Medical Technologies, LLC
Free shipping on orders over $99 · 30-day returns
CHEVEUX DIODE LASER SYSTEM is an FDA 510(k)-cleared medical device (K100893) manufactured by Sandstone Medical Technologies, LLC. 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 15, 2010. Regulation: 8.
