
Precision Biometrics, Inc.
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MYOVISION 3.0 WIREFREE SYSTEM is an FDA 510(k)-cleared medical device (K123399) manufactured by Precision Biometrics, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 31, 2013. Regulation: 8.