BIOPSY FORCEP (NON-ELECTRIC)

BIOPSY FORCEP (NON-ELECTRIC) is an FDA 510(k)-cleared medical device (K896147) manufactured by Portlyn Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 15, 1990. Regulation: 8.