510(k) K030856 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
ER800 SERIES ECG EVENT RECORDER
| Applicant | Braemar Corp., Burnsville MN, US |
| Decision | Substantially Equivalent, Mar 28, 2003 |
| Received | Mar 18, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030856
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.