Cooper Lasersonics, Inc.
MODEL 4000 ND:YAG LASER FOR GENITOURINARY APPLICAT
SKU K850779UPC GEX
In Stock
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IIFDA 510(k) Cleared (K850779)
1
Free shipping on orders over $99 · 30-day returns
Cooper Lasersonics, Inc.
Free shipping on orders over $99 · 30-day returns
MODEL 4000 ND:YAG LASER FOR GENITOURINARY APPLICAT is an FDA 510(k)-cleared medical device (K850779) 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 April 1, 1985. Regulation: 8.
