510(k) K160610 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
Kobold Fletcher-model Tandem and Ovoid Applicator Set, Kobold Henschke-model Tandem and Ovoid Applicator Set, Kobold Vaginal Cylinder Applicator Set, Kobold Miami Cylinder Applicator Set
| Applicant | Kobold, LLC, Veradale WA, US |
| Decision | Substantially Equivalent, Feb 13, 2017 |
| Received | Mar 3, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160610
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.