Candela Corp.
CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS: 532 AND 1064 ND:YAG HANDPIECE ACCESSORIES
SKU K063072UPC GEX
In Stock
—
IIFDA 510(k) Cleared (K063072)
1
Free shipping on orders over $99 · 30-day returns
Candela Corp.
Free shipping on orders over $99 · 30-day returns
CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS: 532 AND 1064 ND:YAG HANDPIECE ACCESSORIES is an FDA 510(k)-cleared medical device (K063072) manufactured by Candela 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 December 19, 2006. Regulation: 8.
