510(k) K101024 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
KENZ CARDY302 MAX
| Applicant | Suzuken Co., Ltd., Richardson TX, US |
| Decision | Substantially Equivalent, Jan 6, 2011 |
| Received | Apr 13, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101024
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.