SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS

SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K946238) manufactured by Symbiosis Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 19, 1995. Regulation: 8.