Danville Materials, Inc.
PRELUDE
SKU K040952UPC KLE
In Stock
—
IIFDA 510(k) Cleared (K040952)
1
Free shipping on orders over $99 · 30-day returns
Danville Materials, Inc.
Free shipping on orders over $99 · 30-day returns
PRELUDE is an FDA 510(k)-cleared medical device (K040952) manufactured by Danville Materials, 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 June 28, 2004. Regulation: 8.
