510(k) K973833 ยท IZL System, X-Ray, Mobile
CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUAL
| Applicant | Dynarad Corp., Deer Park NY, US |
| Decision | Substantially Equivalent, Dec 30, 1997 |
| Received | Oct 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973833
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.