THE TULIP COMPANY WEIL-BLAKESLEY FORCEPS

THE TULIP COMPANY WEIL-BLAKESLEY FORCEPS is an FDA 510(k)-cleared medical device (K952954) manufactured by The Tulip Mfg. Co.. 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 October 29, 1995. Regulation: 8.