510(k) K790739 ยท DPS Electrocardiograph
QUINTON MODEL 530X ECG DATA CART
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 26, 1979 |
| Received | Apr 16, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790739
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.