PRIMUS INSULATED FORCEPS

PRIMUS INSULATED FORCEPS is an FDA 510(k)-cleared medical device (K932832) manufactured by Marlo Surgical Technology. 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 February 24, 1994. Regulation: 8.