E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120

E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120 is an FDA 510(k)-cleared medical device (K961301) manufactured by Delphi Consulting Group. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 10, 1996. Regulation: 8.