Intra Lase Corp.
PULSION FS LASER KERATOME
SKU K013941UPC GEX
In Stock
—
IIFDA 510(k) Cleared (K013941)
1
Free shipping on orders over $99 · 30-day returns
Intra Lase Corp.
Free shipping on orders over $99 · 30-day returns
PULSION FS LASER KERATOME is an FDA 510(k)-cleared medical device (K013941) manufactured by Intra Lase Corp.. 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 February 26, 2002. Regulation: 8.
