510(k) K902535

SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM by Sony Medical Electronics Co. — Product Code JAA

K902535 is an FDA 510(k) premarket notification submitted by Sony Medical Electronics Co. for the device "SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM". The FDA issued a decision of Substantially Equivalent on June 29, 1990. The device falls under product code JAA (System, X-Ray, Fluoroscopic, Image-Intensified), a Class II device regulated under 21 CFR 892.1650. Sony Medical Electronics Co. has at least 7 other 510(k) clearances on record.