510(k) K092323 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
CONTURA CAVITY MAINTENANCE CATHETER
| Applicant | Senorx, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 19, 2009 |
| Received | Aug 4, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092323
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.