SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPS

SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K931957) 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 February 27, 1994. Regulation: 8.