510(k) K896772 ยท DPS Electrocardiograph
EKG, ECG KENZ, ECG 303
| Applicant | Cambridge Medical Instruments, Inc., Ossining NY, US |
| Decision | Substantially Equivalent, Feb 26, 1990 |
| Received | Dec 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896772
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.