FORCEPS, BIOPSY, NON-ELECTRIC

FORCEPS, BIOPSY, NON-ELECTRIC is an FDA 510(k)-cleared medical device (K952863) manufactured by Annex Medical, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 18, 1995. Regulation: 8.