510(k) K031273 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
AMERITEK SURE-POINT HDR NEEDLE TEMPLATE
| Applicant | Amertek Medical, Inc., Singer Island FL, US |
| Decision | Substantially Equivalent, Jul 15, 2003 |
| Received | Apr 22, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031273
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.