510(k) K953046 ยท IYE Accelerator, Linear, Medical
PERI-PUSHER
| Applicant | Diacor, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 22, 1995 |
| Received | Jun 30, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953046
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.