CARTER-THOMASON NEEDLE-POINT SUTURE PASSER

CARTER-THOMASON NEEDLE-POINT SUTURE PASSER is an FDA 510(k)-cleared medical device (K933536) manufactured by Neimark Labs, Inc.. 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 November 21, 1993. Regulation: 8.