510(k) K173226 ยท DPS Electrocardiograph
CardiMax Electrocardiograph
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Apr 16, 2018 |
| Received | Oct 3, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173226
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.