
Lazarus Medical, LLC
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PHONERIS INNER CANNULAE WITH PHONERIS AERO-FLEX VENTILATOR CIRCUIT CONNECTOR is an FDA 510(k)-cleared medical device (K073702) manufactured by Lazarus Medical, LLC. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 25, 2008. Regulation: 8.