Cooper Lasersonics, Inc.
MODELS 4000/6000/8000/8900 LASER FOR DERMA/SURGERY
SKU K873790UPC GEX
In Stock
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IIFDA 510(k) Cleared (K873790)
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Free shipping on orders over $99 · 30-day returns
Cooper Lasersonics, Inc.
Free shipping on orders over $99 · 30-day returns
MODELS 4000/6000/8000/8900 LASER FOR DERMA/SURGERY is an FDA 510(k)-cleared medical device (K873790) manufactured by Cooper Lasersonics, Inc.. 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 January 21, 1988. Regulation: 8.
