510(k) K993618 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
DXP1000 HOLTER RECORDER
| Applicant | Braemar Corp., Burnsville MN, US |
| Decision | Substantially Equivalent, Nov 24, 1999 |
| Received | Oct 26, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K993618
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.