510(k) K173952 ยท DPS Electrocardiograph
Universal SmartECG
| Applicant | Vectracor, Inc., Totowa NJ, US |
| Decision | Substantially Equivalent, Aug 28, 2018 |
| Received | Dec 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173952
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.