VANGUARD REPROCESSED NON-ELECTRIC BIOPSY FORCEPS

VANGUARD REPROCESSED NON-ELECTRIC BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K042594) manufactured by Vanguard Medical Concepts, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 24, 2005. Regulation: 8.