510(k) K890875 ยท DPS Electrocardiograph
CARDIOTEST EK53/EK53R, CARDIOGNOST EK56/EK512
| Applicant | Ppg Industries, Inc., Pleasantville NY, US |
| Decision | Substantially Equivalent, Oct 17, 1989 |
| Received | Feb 21, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890875
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.