510(k) K961092 ยท LNH System, Nuclear Magnetic Resonance Imaging
VISART
| Applicant | Toshiba America Medical Systems, In.C, Tustin CA, US |
| Decision | Substantially Equivalent, Jun 14, 1996 |
| Received | Mar 19, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961092
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 13, 2005 | Toshiba American Med Sys Inc Magnetic Resonance Imaging Systems;
Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN & Excelart VANTAGE. Terminated |
LNH | None listed |
| Dec 2, 2004 | Toshiba American Med Sys Inc Magnetic Resonance Imaging Systems under the following names:
Visart
Excelart
Excelart P2
Excelart P3
Excelart SPIN
Excelart VANTAGE Terminated |
LNH | None listed |
| Jul 20, 2004 | Toshiba American Med Sys Inc Magnetic Resonance Imaging, System: Flexart, Visart and Excelart Models. Terminated |
LNH | None listed |
| Jul 20, 2004 | Toshiba American Med Sys Inc Magnetic Resonance Imaging
System Core Software,
Software installed in all of the following:
Flexart MRI System,
Visart MRI System,
Exelart / Exelart P2 / Exelart P3 SPIN & Exelart VANTAGE MRI Syst Terminated |
LNH | None listed |
| Jul 20, 2004 | Toshiba American Med Sys Inc Magnetic Resonance Imaging System(s)
Visart and Exelart P2/ Exelart P3/ Exelart SPIN and Exelart VANTAGE Terminated |
LNH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.