ClearanceBrief
510(k) K063130 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

APLIO XG DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SSA-790A, VERSION 1.0

ApplicantToshibamedical Systems Corporation, Tustin CA, US
DecisionSubstantially Equivalent, Nov 2, 2006
ReceivedOct 13, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063130

DateFirm and productCodeLinked 510(k)
Jan 9, 2008Toshiba American Med Sys Inc
Toshiba Aplio XG Diagnostic Ultrasound System, Model: SSA-790A with version 1.1 software, Toshiba America Medical Systems, Inc., Tustin, CA. 92780
Terminated
IYNNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.