ANS 2000 ECG MONITOR AND RESPIRATION PACER

ANS 2000 ECG MONITOR AND RESPIRATION PACER is an FDA 510(k)-cleared medical device (K973426) manufactured by D. E. Hokanson, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 11, 1998. Regulation: 8.