Ranfac Cartilage Biopsy Needle

Ranfac Cartilage Biopsy Needle is an FDA 510(k)-cleared medical device (K183146) manufactured by Ranfac Corporation. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 24, 2019. Regulation: 8.