SONICAID MODEL TEAM FECG IUP

SONICAID MODEL TEAM FECG IUP is an FDA 510(k)-cleared medical device (K930714) manufactured by Oxford Instruments, Plc.. 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 23, 1995. Regulation: 8.