Leach and Dillon Co., Inc.
MONOGRAM II
SKU K895064UPC EJT
In Stock
—
IIFDA 510(k) Cleared (K895064)
1
Free shipping on orders over $99 · 30-day returns
Leach and Dillon Co., Inc.
Free shipping on orders over $99 · 30-day returns
MONOGRAM II is an FDA 510(k)-cleared medical device (K895064) manufactured by Leach and Dillon Co., Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 17, 1989. Regulation: 8.
