510(k) K913908 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
OMNITRON GYN APPLICATOR SYSTEM
| Applicant | Omnitron Intl., Inc., Houston TX, US |
| Decision | Substantially Equivalent, Mar 6, 1992 |
| Received | Aug 30, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913908
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.