AMNIOINFUSION CATHETER

AMNIOINFUSION CATHETER is an FDA 510(k)-cleared medical device (K862182) manufactured by Michael Reese Hospital and Medical Center. 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 August 24, 1986. Regulation: 8.