510(k) K081179 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
MAMMOSITE CAVITY EVALUATION DEVICE
| Applicant | Hologic, Inc., Malborough MA, US |
| Decision | Substantially Equivalent, May 9, 2008 |
| Received | Apr 25, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081179
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.