510(k) K132206 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone
MELYS ATRIAL FIBRILLATION SCREENING MONITOR
| Applicant | Advanced Fluidics, LLC, Crofton MD, US |
| Decision | Substantially Equivalent, Mar 19, 2014 |
| Received | Jul 16, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132206
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.