POWER PACK 160 SIEMENS-ELEMA AB

POWER PACK 160 SIEMENS-ELEMA AB is an FDA 510(k)-cleared medical device (K844590) manufactured by Siemens Elema AB. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 28, 1984. Regulation: 8.