510(k) K131503 ยท DPS Electrocardiograph
SE-601 SERIES ELECTROCARDIOGRAPH
| Applicant | Edan Instruments, Inc., Shenzhen, Guangdong, CN |
| Decision | Substantially Equivalent, Feb 25, 2014 |
| Received | May 24, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131503
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.