COLLINS DIGITAL PULMONARY MANOMETER

COLLINS DIGITAL PULMONARY MANOMETER is an FDA 510(k)-cleared medical device (K912946) manufactured by Warren E. Collins, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 14, 1992. Regulation: 8.