510(k) K172611 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled
Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Sets, odd lengths and even lengths, Universal Titanium Cervix Probe Sets, odd lengths and even lengths
| Applicant | Varian Medical Systems, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Mar 21, 2018 |
| Received | Aug 31, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172611
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.