510(k) K170182 ยท DPS Electrocardiograph
CARDIOVIT FT-1
| Applicant | Schiller AG, Baar, CH |
| Decision | Substantially Equivalent, Jul 19, 2017 |
| Received | Jan 23, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170182
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.