
Lasermatic, Inc.
Free shipping on orders over $99 · 30-day returns
MODEL 5050 SURGILASER FOR PULMONARY USE is an FDA 510(k)-cleared medical device (K871876) manufactured by Lasermatic, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 21, 1988. Regulation: 8.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031