Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human

Cordis, A Johnson & Johnson Co.
Free shipping on orders over $99 · 30-day returns
CORDIS AVIATOR PERIPHERAL DILATATION CATHETER is an FDA 510(k)-cleared medical device (K013581) manufactured by Cordis, A Johnson & Johnson Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 27, 2001. Regulation: 8.