
Vygon Corp.
Free shipping on orders over $99 · 30-day returns
VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW is an FDA 510(k)-cleared medical device (K851480) manufactured by Vygon Corp.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 6, 1985. Regulation: 8.