Candela Laser Corp.
CANDELA Q-SWITCHED ALEXANDRITE LASERS
SKU K955662UPC GEX
In Stock
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IIFDA 510(k) Cleared (K955662)
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Free shipping on orders over $99 · 30-day returns
Candela Laser Corp.
Free shipping on orders over $99 · 30-day returns
CANDELA Q-SWITCHED ALEXANDRITE LASERS is an FDA 510(k)-cleared medical device (K955662) manufactured by Candela 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 June 13, 1996. Regulation: 8.
