510(k) K180234 ยท DPS Electrocardiograph
physiQ Heart Rhythm Module
| Applicant | Physiq, Inc., Naperville IL, US |
| Decision | Substantially Equivalent, Aug 10, 2018 |
| Received | Jan 29, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180234
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.