Candela Corp.
CANDELA GENTLELASE GL DERMATOLOGICAL VASCULAR LESION LASER
SKU K972767UPC GEX
In Stock
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IIFDA 510(k) Cleared (K972767)
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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 GENTLELASE GL DERMATOLOGICAL VASCULAR LESION LASER is an FDA 510(k)-cleared medical device (K972767) 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 3, 1997. Regulation: 8.
