510(k) K060349 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
PROGUIDE NEEDLE SET
| Applicant | Nucletron Corporation, Columbia MD, US |
| Decision | Substantially Equivalent, Mar 10, 2006 |
| Received | Feb 10, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060349
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.