510(k) K091856 ยท DRX Electrode, Electrocardiograph
CONMED ECG MONITORING ELECTRODES , MODEL 1700 ( INCLUDING 2500), 1750, 2700, 2710, 1800, SERIES
| Applicant | Conmed Corporation, Utica NY, US |
| Decision | Substantially Equivalent, Aug 7, 2009 |
| Received | Jun 23, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091856
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.