510(k) K171244 ยท DRX Electrode, Electrocardiograph
Physiotrace
| Applicant | Nimbleheart, Inc., Campbell CA, US |
| Decision | Substantially Equivalent, Aug 23, 2017 |
| Received | Apr 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171244
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.