510(k) K130921 ยท DPS Electrocardiograph
ALIVECOR HEART MONITOR OTC
| Applicant | AliveCor, Inc., San Francisco CA, US |
| Decision | Substantially Equivalent, Feb 6, 2014 |
| Received | Apr 3, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130921
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.