Laserguide
SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE
SKU K873892UPC LNK
In Stock
—
IIFDA 510(k) Cleared (K873892)
1
Free shipping on orders over $99 · 30-day returns
Laserguide
Free shipping on orders over $99 · 30-day returns
SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE is an FDA 510(k)-cleared medical device (K873892) manufactured by Laserguide. 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 1, 1988. Regulation: 8.
