510(k) K971380 ยท LNH System, Nuclear Magnetic Resonance Imaging
MEDRAD FLEX INTERFACE DEVICE
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Jul 3, 1997 |
| Received | Apr 14, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971380
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.