510(k) K961400 ยท IYE Accelerator, Linear, Medical
RFA-300, LDA UTILITY
| Applicant | Scanditronix Medical AB, Towaco NJ, US |
| Decision | Substantially Equivalent, Jan 3, 1997 |
| Received | Apr 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961400
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.