510(k) K933018 ยท LNH System, Nuclear Magnetic Resonance Imaging
MRT-50GP
| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Feb 18, 1994 |
| Received | Jun 22, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933018
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| 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 |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.