510(k) K821758 ยท DPS Electrocardiograph
QUINTON Q, SCAN MODELS 900 & 901
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 25, 1982 |
| Received | Jun 15, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821758
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.