ClearanceBrief
510(k) K090158 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

APLIO ARTIDA V2.0 SSH-880CV

ApplicantToshiba America Medical Systems, In.C, Tustin CA, US
DecisionSubstantially Equivalent, Feb 6, 2009
ReceivedJan 22, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090158

DateFirm and productCodeLinked 510(k)
Jul 29, 2011Toshiba American Medical Systems Inc
Aplio Artida Ultrasound Diagnostic System SSH-880CV. Toshiba American Medical Systems, Inc. A diagnostic ultrasound system.
Terminated
IYNNone listed
May 19, 2011Toshiba American Medical Systems Inc
Software for SSH-880CV Aplio Artida; System Diagnostic Ultrasound
Terminated
IYNNone listed
May 10, 2011Toshiba American Medical Systems Inc
Toshiba America Medical Systems Inc. SSH-880CV Aplio Artida; Diagnostic Ultrasound System
Terminated
IYNNone listed
Mar 3, 2011Toshiba American Medical Systems Inc
SSH-880CV Aplio Artida; System, Diagnostic Ultrasound
Terminated
IYONone listed
Jul 6, 2010Toshiba American Medical Systems Inc
SSH-880CV Aplio Artida System
Terminated
IYONone listed

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