OLYMPUS FB SERIES BIOPSY FORCEPS

OLYMPUS FB SERIES BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K955065) manufactured by Olympus America, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 23, 1996. Regulation: 8.