ACCUSTRESS EXERCISE TESTING SYSTEM

ACCUSTRESS EXERCISE TESTING SYSTEM is an FDA 510(k)-cleared medical device (K953127) manufactured by Hewlett-Packard Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 1996. Regulation: 8.