510(k) K082264 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
CONTURA LUMEN MARKER
| Applicant | Senorx, Inc., Aliso Viejo CA, US |
| Decision | Unknown, Sep 12, 2008 |
| Received | Aug 11, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082264
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.