510(k) K120300 ยท JAK System, X-Ray, Tomography, Computed
CT-GUIDE NEEDLE GUIDANCE SYSTEM
| Applicant | Activiews, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Apr 13, 2012 |
| Received | Jan 31, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120300
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.