510(k) K012154 ยท LNH System, Nuclear Magnetic Resonance Imaging
AURORA MAGNETIC RESONANCE DIAGNOSTIC DEVICE
| Applicant | Aurora Imaging Technology, Inc., North Andover MA, US |
| Decision | Substantially Equivalent, Sep 19, 2001 |
| Received | Jul 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012154
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.