510(k) K954310 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
BLA-800A
| Applicant | Toshiba Medical Systems, Tustin CA, US |
| Decision | Substantially Equivalent, Oct 18, 1995 |
| Received | Sep 15, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954310
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.