510(k) K080934 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
VIENNA RING CT/MR APPLICATOR SET, ROUND POINT TITANIUM NEEDLE SET, TROCAR POINT TITANIUM NEEDLE SET
| Applicant | Nucletron Corporation, Columbia MD, US |
| Decision | Substantially Equivalent, May 28, 2008 |
| Received | Apr 2, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080934
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.