Kavo America
KAVO POLYLUX II
SKU K013500UPC EBZ
In Stock
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IIFDA 510(k) Cleared (K013500)
1
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Kavo America
Free shipping on orders over $99 · 30-day returns
KAVO POLYLUX II is an FDA 510(k)-cleared medical device (K013500) manufactured by Kavo America. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 13, 2002. Regulation: 8.
