510(k) K935691 ยท LNH System, Nuclear Magnetic Resonance Imaging
MODEL GP-252 GENERAL PURPOSE COIL
| Applicant | Diagnostic Instrument Corp., Aurora OH, US |
| Decision | Substantially Equivalent, Aug 1, 1994 |
| Received | Nov 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935691
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.