ANGIOSCOPE FOR PULMONARY ARTERY USE

ANGIOSCOPE FOR PULMONARY ARTERY USE is an FDA 510(k)-cleared medical device (K882658) manufactured by Washington Regulatory Services. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 1989. Regulation: 8.