TISCHLER BIOPSY FORCEPS

TISCHLER BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K926538) manufactured by Thomasville Medical Assoc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 23, 1994. Regulation: 8.