PERRYMETER(TM)

PERRYMETER(TM) is an FDA 510(k)-cleared medical device (K911190) manufactured by Perrymeter Systems. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 25, 1991. Regulation: 8.