510(k) K011729 ยท DTC Analyzer, Pacemaker Generator Function
SIGMA PACE EXTERNAL PACEMAKER ANALYZER MODEL #1000
| Applicant | Dni Nevada, Inc., Carson City NV, US |
| Decision | Substantially Equivalent, Aug 30, 2001 |
| Received | Jun 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011729
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.