Minnesota Laser Corp.
PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG
SKU K854469UPC GEX
In Stock
—
IIFDA 510(k) Cleared (K854469)
1
Free shipping on orders over $99 · 30-day returns
Minnesota Laser Corp.
Free shipping on orders over $99 · 30-day returns
PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG is an FDA 510(k)-cleared medical device (K854469) 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.
