510(k) K891541 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETIC RESONANCE DEVICE ACCESSORY SOFTWARE 4.0.
| Applicant | Diasonics, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, May 11, 1989 |
| Received | Mar 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891541
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.