I.V. CATHETER PLACEMENT UNIT POLYURETH

I.V. CATHETER PLACEMENT UNIT POLYURETH is an FDA 510(k)-cleared medical device (K830972) manufactured by Critikon Company, LLC. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 26, 1983. Regulation: 8.