SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND

SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND is an FDA 510(k)-cleared medical device (K932265) 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 August 8, 1993. Regulation: 8.