510(k) K902984 ยท IZL System, X-Ray, Mobile
G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITS
| Applicant | Electromek Diagnostic Systems, Inc., Troy IL, US |
| Decision | Substantially Equivalent, Oct 26, 1990 |
| Received | Jun 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902984
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.