Pelikan Technologies, Inc.
L1-PRO SYSTEM
SKU K041665UPC FMK
In Stock
—
IIFDA 510(k) Cleared (K041665)
1
Free shipping on orders over $99 · 30-day returns
Pelikan Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
L1-PRO SYSTEM is an FDA 510(k)-cleared medical device (K041665) manufactured by Pelikan Technologies, 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 July 22, 2004. Regulation: 8.
