
E-Med Innovations, Inc.
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E-STETH ELECTRONIC STETHOSCOPE is an FDA 510(k)-cleared medical device (K011898) manufactured by E-Med Innovations, 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 September 13, 2001. Regulation: 8.