CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI

CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI is an FDA 510(k)-cleared medical device (K924530) manufactured by Cabot Medical Corp.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 4, 1993. Regulation: 8.