510(k) K001896 ยท DPS Electrocardiograph
KENZ ECG 108 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS; KENZ ECG 110 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS WITH EC
| Applicant | Suzuken Co., Ltd., Great Neck NY, US |
| Decision | Substantially Equivalent, Jan 8, 2001 |
| Received | Jun 21, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001896
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.