MODIFIED FLOCATH PULMONARY ARTERY CATHETER

MODIFIED FLOCATH PULMONARY ARTERY CATHETER is an FDA 510(k)-cleared medical device (K901733) manufactured by Cardio Metrics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 15, 1990. Regulation: 8.