Utah Medical Products, Inc.
FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+)
SKU K123310UPC GEI
In Stock
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IIFDA 510(k) Cleared (K123310)
1
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Utah Medical Products, Inc.
Free shipping on orders over $99 · 30-day returns
FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+) is an FDA 510(k)-cleared medical device (K123310) manufactured by Utah Medical Products, 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 22, 2013. Regulation: 8.
