MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000

MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000 is an FDA 510(k)-cleared medical device (K982889) manufactured by Electromed, 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 May 31, 1999. Regulation: 8.