510(k) K110812 ยท JAK System, X-Ray, Tomography, Computed
CT-GUIDE NEEDLE GUIDANCE SYSTEM
| Applicant | Activiews, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Jun 21, 2011 |
| Received | Mar 23, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110812
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.