510(k) K171943 ยท DPS Electrocardiograph
Electrocardiograph
| Applicant | Edan Instruments, Inc., Shenzhen, CN |
| Decision | Substantially Equivalent, Sep 25, 2017 |
| Received | Jun 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171943
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.