510(k) K082709 ยท DPS Electrocardiograph
VICOR PD2I ANALYZER, VERSION 2.1
| Applicant | Vicor Technologies, Inc., New York NY, US |
| Decision | Substantially Equivalent, Dec 29, 2008 |
| Received | Sep 16, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082709
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.