510(k) K902988 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
G.E. MSI 850/850II/1250 THREE PHASE GENERATORS
| Applicant | Electromek Diagnostic Systems, Inc., Troy IL, US |
| Decision | Substantially Equivalent, Dec 19, 1990 |
| Received | Jun 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902988
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.