Minnesota Laser Corp.
PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG
SKU K854472UPC GEX
In Stock
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IIFDA 510(k) Cleared (K854472)
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Free shipping on orders over $99 · 30-day returns
Minnesota Laser Corp.
Free shipping on orders over $99 · 30-day returns
PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG is an FDA 510(k)-cleared medical device (K854472) manufactured by Minnesota Laser Corp.. 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 10, 1986. Regulation: 8.
