Resectr Tissue Resection Device

Resectr Tissue Resection Device is an FDA 510(k)-cleared medical device (K191538) manufactured by Boston Scientific Corporation. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 15, 2020. Regulation: 8.