510(k) K933613 ยท IYE Accelerator, Linear, Medical
3-WAY HEAD IMMOBILIZER; 3WAY DELUXE REUSABLE FRAME HEAD IMMOBILIZER
| Applicant | Bionix Development Corp., Toledo OH, US |
| Decision | Substantially Equivalent, Oct 7, 1993 |
| Received | Jul 19, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933613
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.