AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO

AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO is an FDA 510(k)-cleared medical device (K001502) manufactured by Erich Jaeger GmbH. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 11, 2000. Regulation: 8.