510(k) K051765 ยท JAK System, X-Ray, Tomography, Computed
CERETOM, MODEL NL3000
| Applicant | Neurologica Corporation, Danvers MA, US |
| Decision | Substantially Equivalent, Jul 14, 2005 |
| Received | Jun 30, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051765
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.