510(k) K911775 ยท KXK Source, Brachytherapy, Radionuclide
OMNICATH IMPLANTED CATHETER AND DEPOT
| Applicant | Omnitron Intl., Inc., Houston TX, US |
| Decision | Substantially Equivalent, May 8, 1991 |
| Received | Apr 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911775
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.