510(k) K032490 ยท LNH System, Nuclear Magnetic Resonance Imaging
TOSHIBA EXCELART VANTAGE XGV/AGV MRI DIAGNOSTIC SYSTEM, MODELS MRT-1503/P3 AND MRT-1503/P2
| Applicant | Toshiba America Medical Systems, In.C, Tustin CA, US |
| Decision | Substantially Equivalent, Aug 21, 2003 |
| Received | Aug 12, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032490
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 28, 2012 | Toshiba American Medical Systems Inc EXCELART Vantage, Atlas, and Titan MRI Systems, MRT-1503 and MRT-1504.
Imaging of the Whole Body, Fluid Visualization, 2D/3D Imaging, MR Angiography/MR Vascular Imaging, Blood Oxygenation Level Depen Terminated |
LNH | None listed |
| Dec 14, 2005 | Toshiba American Med Sys Inc Toshiba Excelart VANTAGE Model MRT-1503, Magnetic Resonance Imaging Systems, Regulation Number 21 CPR 892.1000, Regulatory Class II, Product Code 90-LNH and was cleared with K032490 Terminated |
LNH | None listed |
| Nov 2, 2004 | Toshiba American Med Sys Inc Excelart (tm) VANTAGE P2 & P3, Magnetic Resonance Imaging System, Terminated |
LNH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.