510(k) K893660 ยท DPS Electrocardiograph
ECG SIMULATOR MODEL ECGPLUS
| Applicant | Bio-Tek Instruments, Inc., Winooski VT, US |
| Decision | Substantially Equivalent, Dec 5, 1989 |
| Received | May 15, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893660
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.