510(k) K932292 ยท LNH System, Nuclear Magnetic Resonance Imaging
AUTOTUNE DEVICE (ATD II) FOR PICKER MRI SYSTEMS
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Aug 26, 1993 |
| Received | May 10, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932292
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.