510(k) K032372 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
NUCLETRON COMFORT CATHETER SYSTEM, MODEL 189.007
| Applicant | Nucletron Corporation, Columbia MD, US |
| Decision | Substantially Equivalent, Aug 15, 2003 |
| Received | Aug 1, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032372
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.