Candela Corp.
CANDELA FAMILY OF PULSED DYE LASER SYSTEMS: PIGMENTED LESION HANDPIECE ACCESSORY
SKU K051359UPC GEX
In Stock
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IIFDA 510(k) Cleared (K051359)
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Free shipping on orders over $99 · 30-day returns
Candela Corp.
Free shipping on orders over $99 · 30-day returns
CANDELA FAMILY OF PULSED DYE LASER SYSTEMS: PIGMENTED LESION HANDPIECE ACCESSORY is an FDA 510(k)-cleared medical device (K051359) 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 July 12, 2005. Regulation: 8.
