PERCUSSIVETECH HF, MODEL 2001

PERCUSSIVETECH HF, MODEL 2001 is an FDA 510(k)-cleared medical device (K981726) manufactured by Vortran Medical Technology 1, 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 September 16, 1998. Regulation: 8.