510(k) K133014 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
DMS 300-2W HOLTER ECG RECORDER
| Applicant | Diagnostic Monitoring Software, Stateline NV, US |
| Decision | Substantially Equivalent, May 19, 2014 |
| Received | Sep 25, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133014
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.