Lutronic Corporation
SPECTRA LASER SYSTEM
SKU K113588UPC GEX
In Stock
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IIFDA 510(k) Cleared (K113588)
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Free shipping on orders over $99 · 30-day returns
Lutronic Corporation
Free shipping on orders over $99 · 30-day returns
SPECTRA LASER SYSTEM is an FDA 510(k)-cleared medical device (K113588) manufactured by Lutronic Corporation. 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 February 21, 2012. Regulation: 8.
