American Laser Medical
NUVOLASE 532 CUTANEOUS LASER SYSTEM
SKU K990780UPC GEX
In Stock
—
IIFDA 510(k) Cleared (K990780)
1
Free shipping on orders over $99 · 30-day returns
American Laser Medical
Free shipping on orders over $99 · 30-day returns
NUVOLASE 532 CUTANEOUS LASER SYSTEM is an FDA 510(k)-cleared medical device (K990780) manufactured by American Laser Medical. 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 March 21, 1999. Regulation: 8.
