510(k) K030051 ยท IYE Accelerator, Linear, Medical
VERSABOARD, MODEL 7040
| Applicant | Bionix Development Corp., Toledo OH, US |
| Decision | Substantially Equivalent, Apr 4, 2003 |
| Received | Jan 6, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030051
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.