510(k) K000209 ยท IYE Accelerator, Linear, Medical
DOSE 1
| Applicant | Scanditronix Wellhofer North America, Bartlett TN, US |
| Decision | Substantially Equivalent, Aug 18, 2000 |
| Received | Jan 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000209
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.