VALLEY FORGE BIPOLAR LOOP

VALLEY FORGE BIPOLAR LOOP is an FDA 510(k)-cleared medical device (K971986) manufactured by Valley Forge Scientific Corp.. 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 August 25, 1997. Regulation: 8.