510(k) K873584 ยท DPS Electrocardiograph
MODIFIED Q4000 & Q3040 ELECTROCARDIOGRAPH MONITOR
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Oct 26, 1987 |
| Received | Sep 4, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873584
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.