510(k) K935021 ยท IYE Accelerator, Linear, Medical
HANDI-FOAM
| Applicant | Medtec, Inc., Orange City IA, US |
| Decision | Substantially Equivalent, Apr 7, 1994 |
| Received | Oct 20, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935021
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.