DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH

DIAFLEX GRASP FORCEPS/RETRIEVAL LOOP & CYTO BRUSH is an FDA 510(k)-cleared medical device (K881332) manufactured by Baxter Healthcare Corp. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 26, 1988. Regulation: 8.