510(k) K911667 ยท LNH System, Nuclear Magnetic Resonance Imaging
HITACHI MRP-7000 MAGNETIC ROSONANCE DEVICE
| Applicant | Hitachi Medical Systems America, Inc., Twinsburg OH, US |
| Decision | Substantially Equivalent, May 30, 1991 |
| Received | Apr 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911667
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 12, 2006 | Hitachi Medical Systems America Inc MRP-7000 and AIRIS Magnetic Resonance Imaging Systems, Software Versions: V7.0A to V7.0J. Terminated |
LNH | None listed |
| Jun 10, 2006 | Hitachi Medical Systems America Inc MRP-7000, AIRIS Magnetic Resonance Imaging Systems Terminated |
LNH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.