
Heartforce Medical, Inc.
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DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300 is an FDA 510(k)-cleared medical device (K081603) manufactured by Heartforce Medical, 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 July 23, 2009. Regulation: 8.