510(k) K910017 ยท DPS Electrocardiograph
Q4500 STREE TEST MONITOR
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Nov 5, 1991 |
| Received | Jan 3, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910017
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.