510(k) K160840 ยท DPS Electrocardiograph
ECG100+, ECG200+
| Applicant | Cardioline S.P.A, Spini Di Gardolo, IT |
| Decision | Substantially Equivalent, Aug 12, 2016 |
| Received | Mar 28, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160840
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.