PERSYST 12 ( P12) EGG REVIEW AND ANALYSIS SOFTWARE

PERSYST 12 ( P12) EGG REVIEW AND ANALYSIS SOFTWARE is an FDA 510(k)-cleared medical device (K133793) manufactured by Persyst Development Corporation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 18, 2014. Regulation: 8.