510(k) K883468 ยท DPS Electrocardiograph
Q5000 ST/HR SLOPE MODIFICATION
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Dec 27, 1988 |
| Received | Aug 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883468
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.