510(k) K130294 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
BRAEMAR CARDIOKEY HOLTER RECORDER
| Applicant | Braemar Manufacturing, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Oct 16, 2013 |
| Received | Feb 6, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130294
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.