510(k) K992580

FETAL ASSESSMENT CAP by Acuson Corp. — Product Code IYO

K992580 is an FDA 510(k) premarket notification submitted by Acuson Corp. for the device "FETAL ASSESSMENT CAP". The FDA issued a decision of Substantially Equivalent on October 18, 1999. The device falls under product code IYO (System, Imaging, Pulsed Echo, Ultrasonic), a Class II device regulated under 21 CFR 892.1560. Acuson Corp. has at least 10 other 510(k) clearances on record.