Portex NRFit Epidural Needles

Portex NRFit Epidural Needles is an FDA 510(k)-cleared medical device (K172823) manufactured by Smiths Medical Asd, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 11, 2018. Regulation: 8.