FLEXIBLE BIOPSY FORCEPS

FLEXIBLE BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K760717) manufactured by V. Mueller O.V. Baxter Healthcare Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 20, 1976. Regulation: 8.